Tag: 100-200

Kamat, P. V. et al. published their research in Journal of the Indian Chemical Society in 1970 | CAS: 1634-34-0

2′,6′-Dihydroxy-4′-methylacetophenone (cas: 1634-34-0) belongs to alcohols. Alcohols are weak acids. The most acidic simple alcohols (methanol and ethanol) are about as acidic as water, and most other alcohols are somewhat less acidic. Alcohols may be oxidized to give ketones, aldehydes, and carboxylic acids. These functional groups are useful for further reactions. Oxidation of organic compounds generally increases the number of bonds from carbon to oxygen (or another electronegative element, such as a halogen), and it may decrease the number of bonds to hydrogen.Recommanded Product: 2′,6′-Dihydroxy-4′-methylacetophenone

Proton-ligand stability constants of substituted ortho-hydroxyacetophenones and ortho-hydroxypropiophenones was written by Kamat, P. V.;Datar, M. G.. And the article was included in Journal of the Indian Chemical Society in 1970.Recommanded Product: 2′,6′-Dihydroxy-4′-methylacetophenone This article mentions the following:

Proton-ligand stability constant of substituted o-hydroxyacetophenones and o-hydroxypropiophenones were determined at 30° by a potentiometric method by the Bjerrum-Calvin titration technique at constant ionic strength ∼0.1M NaClO4. Correlation between the effect and the position of substituents in the benzene nucleus is discussed. In the experiment, the researchers used many compounds, for example, 2′,6′-Dihydroxy-4′-methylacetophenone (cas: 1634-34-0Recommanded Product: 2′,6′-Dihydroxy-4′-methylacetophenone).

2′,6′-Dihydroxy-4′-methylacetophenone (cas: 1634-34-0) belongs to alcohols. Alcohols are weak acids. The most acidic simple alcohols (methanol and ethanol) are about as acidic as water, and most other alcohols are somewhat less acidic. Alcohols may be oxidized to give ketones, aldehydes, and carboxylic acids. These functional groups are useful for further reactions. Oxidation of organic compounds generally increases the number of bonds from carbon to oxygen (or another electronegative element, such as a halogen), and it may decrease the number of bonds to hydrogen.Recommanded Product: 2′,6′-Dihydroxy-4′-methylacetophenone

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Kisic, Andrea et al. published their research in Advanced Synthesis & Catalysis in 2014 | CAS: 171032-87-4

(S)-1-(2-Fluorophenyl)ethanol (cas: 171032-87-4) belongs to alcohols. A strong base can deprotonate an alcohol to yield an alkoxide ion (R―O−). For example, sodamide (NaNH2), a very strong base, abstracts the hydrogen atom of an alcohol. Tertiary alcohols cannot be oxidized at all without breaking carbon-carbon bonds, whereas primary alcohols can be oxidized to aldehydes or further oxidized to carboxylic acids.Application of 171032-87-4

ansa-Ruthenium(II) Complexes of DPEN-SO2N(Me)(CH2)n(η6-aryl) Conjugate Ligands for Asymmetric Transfer Hydrogenation of Aryl Ketones was written by Kisic, Andrea;Stephan, Michel;Mohar, Barbara. And the article was included in Advanced Synthesis & Catalysis in 2014.Application of 171032-87-4 This article mentions the following:

A diversified ansa-ruthenium(II) catalyst series displaying enantiopure N,C-(N-alkylene-N-methylsulfamoyl)-tethered (DPEN-κ2N,N’)/η6-arene (DPEN = trans-1,2-diphenylethylenediamine) hybrid ligands was screened in the transfer hydrogenation of alkyl aryl ketones and α- or β-diketones in formic acid-triethylamine (HCO2H-Et3N) medium under mild conditions and furnished the alcs. in high to excellent ees. In the experiment, the researchers used many compounds, for example, (S)-1-(2-Fluorophenyl)ethanol (cas: 171032-87-4Application of 171032-87-4).

(S)-1-(2-Fluorophenyl)ethanol (cas: 171032-87-4) belongs to alcohols. A strong base can deprotonate an alcohol to yield an alkoxide ion (R―O−). For example, sodamide (NaNH2), a very strong base, abstracts the hydrogen atom of an alcohol. Tertiary alcohols cannot be oxidized at all without breaking carbon-carbon bonds, whereas primary alcohols can be oxidized to aldehydes or further oxidized to carboxylic acids.Application of 171032-87-4

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Blaszczyk, Alfred et al. published their research in European Journal of Organic Chemistry in 2006 | CAS: 29364-29-2

Sodium 2-methyl-2-propanethiolate (cas: 29364-29-2) belongs to alcohols. A strong base can deprotonate an alcohol to yield an alkoxide ion (R―O−). For example, sodamide (NaNH2), a very strong base, abstracts the hydrogen atom of an alcohol. A multistep synthesis may use Grignard-like reactions to form an alcohol with the desired carbon structure, followed by reactions to convert the hydroxyl group of the alcohol to the desired functionality.Application In Synthesis of Sodium 2-methyl-2-propanethiolate

Synthesis of macrocyclic molecular rods as potential electronic devices was written by Blaszczyk, Alfred;Chadim, Martin;von Haenisch, Carsten;Mayor, Marcel. And the article was included in European Journal of Organic Chemistry in 2006.Application In Synthesis of Sodium 2-methyl-2-propanethiolate This article mentions the following:

The design and synthesis of the macrocycles I (R = H, NO2) as model compounds for the investigation of neg. differential conductance phenomena in mol. junctions are reported. I (R = H, NO2) comprise a mol. rod subunit consisting of three ethynyl-linked Ph rings. While the rotational freedom along the rod axis of both terminal Ph rings is limited by the macrocyclic frame, the central Ph ring is revolving. The rod substructure is terminally functionalized with acetyl-protected thiol groups to enable its immobilization between gold contacts. The central Ph ring is functionalized with one and two nitro groups for I (R = H, NO2). The nitro groups are of particular importance as (i) both macrocycles are model compounds to investigate a hypothetical intramol. interaction of the nitro group with the opposite macrocyclic subunits and (ii) the nitro group(s) result in limited thermal stability of the compounds due to the intramol. rearrangement to macrocycles comprising isatogen subunits. These highly functionalized macrocycles have been assembled by acetylene scaffolding strategies in combination with functional group transformation chem. In the experiment, the researchers used many compounds, for example, Sodium 2-methyl-2-propanethiolate (cas: 29364-29-2Application In Synthesis of Sodium 2-methyl-2-propanethiolate).

Sodium 2-methyl-2-propanethiolate (cas: 29364-29-2) belongs to alcohols. A strong base can deprotonate an alcohol to yield an alkoxide ion (R―O−). For example, sodamide (NaNH2), a very strong base, abstracts the hydrogen atom of an alcohol. A multistep synthesis may use Grignard-like reactions to form an alcohol with the desired carbon structure, followed by reactions to convert the hydroxyl group of the alcohol to the desired functionality.Application In Synthesis of Sodium 2-methyl-2-propanethiolate

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Darvishi, Kamran et al. published their research in Applied Organometallic Chemistry in 2018 | CAS: 1777-82-8

(2,4-Dichlorophenyl)methanol (cas: 1777-82-8) belongs to alcohols. Alcohols are weak acids. The most acidic simple alcohols (methanol and ethanol) are about as acidic as water, and most other alcohols are somewhat less acidic. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.HPLC of Formula: 1777-82-8

Preparation, characterization and heterogeneous catalytic applications of GO/Fe3O4/HPW nanocomposite in chemoselective and green oxidation of alcohols with aqueous H2O2 was written by Darvishi, Kamran;Amani, Kamal;Rezaei, Manuchehr. And the article was included in Applied Organometallic Chemistry in 2018.HPLC of Formula: 1777-82-8 This article mentions the following:

Graphene oxide-Fe3O4-NH3+H2PW12O40– magnetic nanocomposite (GO/Fe3O4/HPW) was prepared by linking amino-functionalized Fe3O4 nanoparticles (Fe3O4-NH2) on the graphene oxide (GO), and then grafting 12-tungstophosphoric acid (H3PW12O40) on the graphene oxide-magnetite hybrid (GO-Fe3O4-NH2). The obtained GO/Fe3O4/HPW nanocomposite was well characterized with different techniques such as FT-IR, TEM, SEM, XRD, EDX, TGA-DTA, AGFM, ICP and BET measurements. The used techniques showed that the graphene oxide layers were well prepared and the various stages of preparation of the GO/Fe3O4/HPW nanocomposites successfully completed. This new nanocomposite displayed excellent performance as a heterogeneous catalyst in the oxidation of alcs. with H2O2. The as-prepared GO/Fe3O4/HPW catalyst was more stable and recyclable at least five times without significantly reducing its catalytic activity. In the experiment, the researchers used many compounds, for example, (2,4-Dichlorophenyl)methanol (cas: 1777-82-8HPLC of Formula: 1777-82-8).

(2,4-Dichlorophenyl)methanol (cas: 1777-82-8) belongs to alcohols. Alcohols are weak acids. The most acidic simple alcohols (methanol and ethanol) are about as acidic as water, and most other alcohols are somewhat less acidic. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.HPLC of Formula: 1777-82-8

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Zheng, Gao-Wei et al. published their research in RSC Advances in 2013 | CAS: 120121-01-9

(R)-1-(3-Chlorophenyl)ethanol (cas: 120121-01-9) belongs to alcohols. Alcohols are among the most common organic compounds. They are used as sweeteners and in making perfumes, are valuable intermediates in the synthesis of other compounds, and are among the most abundantly produced organic chemicals in industry. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.Recommanded Product: (R)-1-(3-Chlorophenyl)ethanol

Separation of enantiopure m-substituted 1-phenylethanols in high space-time yield using Bacillus subtilis esterase was written by Zheng, Gao-Wei;Liu, Xu-Yun;Zhang, Zhi-Jun;Tian, Ping;Lin, Guo-Qiang;Xu, Jian-He. And the article was included in RSC Advances in 2013.Recommanded Product: (R)-1-(3-Chlorophenyl)ethanol This article mentions the following:

A recombinant Bacillus subtilis esterase (BsE) expressed in E. coli was found to exhibit excellent enantioselectivity (E was always greater than 100) towards m-substituted 1-phenylethanol acetates in the enantioselective hydrolysis reaction. An explanation for the high enantioselectivity observed towards these substrates was provided by mol. modeling. Moreover, the BsE also showed strong tolerance towards a high concentration of m-substituted 1-phenylethanol acetates (up to 1 M). Based on these excellent catalytic properties of BsE, a kind of m-substituted 1-phenylethanols, (R)-1-(3-chlorophenyl)ethanol, was efficiently synthesized in space-time yield of 920 g per L per day and 97% ee, indicating that the BsE was considered as a potentially ideal and promising biocatalyst for large-scale production of optically active m-substituted 1-phenylethanols. In the experiment, the researchers used many compounds, for example, (R)-1-(3-Chlorophenyl)ethanol (cas: 120121-01-9Recommanded Product: (R)-1-(3-Chlorophenyl)ethanol).

(R)-1-(3-Chlorophenyl)ethanol (cas: 120121-01-9) belongs to alcohols. Alcohols are among the most common organic compounds. They are used as sweeteners and in making perfumes, are valuable intermediates in the synthesis of other compounds, and are among the most abundantly produced organic chemicals in industry. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.Recommanded Product: (R)-1-(3-Chlorophenyl)ethanol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Gedik, Osman et al. published their research in South African Journal of Botany in 2022 | CAS: 499-75-2

5-Isopropyl-2-methylphenol (cas: 499-75-2) belongs to alcohols. Alcohols are weak acids. The most acidic simple alcohols (methanol and ethanol) are about as acidic as water, and most other alcohols are somewhat less acidic. Tertiary alcohols cannot be oxidized at all without breaking carbon-carbon bonds, whereas primary alcohols can be oxidized to aldehydes or further oxidized to carboxylic acids.Reference of 499-75-2

Determining the essential oil components and plant nutrient element values of some Satureja genotypes was written by Gedik, Osman;Kocabas, Yusuf Ziya;Cinar, Orcun. And the article was included in South African Journal of Botany in 2022.Reference of 499-75-2 This article mentions the following:

The essential oil components and plant nutrient element values of a total of 4 different genotypes of two different species in the genus Satureja were determined in the present study. Nurhak, Baskonus, and Kapidere genotypes were classified as belonging to Satureja hortensis L., and Goksun genotype to Satureja cuneifolia Ten. The plant samples of the genotypes were taken during the flowering period, dried in the shade, and the resulting herbals were used for essential oil extraction and plant nutrient identification. The essential oil ratio among the genotypes was between 1.83-3.00% and the highest essential oil ratio was obtained from the Baskonus genotype with 3.00%. A total of 27 different components were determined in the essential oil of the genotypes, and the main components were found to be carvacrol (5.28-64.00%) and thymol (0.28-40.96%), -terpinene (17.23-32.36%), and cymene (7.78-16.80%). Regarding the plant nutrients, the highest Ca, Mn, Fe, and Mg values were found in Kapidere genotype; Zn, Na, and P in Baskonus genotype, K in Nurhak and Baskonus genotypes, and the highest Cu was detected in Nurhak genotype. Baskonus genotype stood out in terms of essential oil and carvacrol ratios. In the experiment, the researchers used many compounds, for example, 5-Isopropyl-2-methylphenol (cas: 499-75-2Reference of 499-75-2).

5-Isopropyl-2-methylphenol (cas: 499-75-2) belongs to alcohols. Alcohols are weak acids. The most acidic simple alcohols (methanol and ethanol) are about as acidic as water, and most other alcohols are somewhat less acidic. Tertiary alcohols cannot be oxidized at all without breaking carbon-carbon bonds, whereas primary alcohols can be oxidized to aldehydes or further oxidized to carboxylic acids.Reference of 499-75-2

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Pham, Hoai Linh Linh et al. published their research in Journal of Sol-Gel Science and Technology in 2022 | CAS: 111-46-6

2,2′-Oxybis(ethan-1-ol) (cas: 111-46-6) belongs to alcohols. Similar to water, an alcohol can be pictured as having an sp3 hybridized tetrahedral oxygen atom with nonbonding pairs of electrons occupying two of the four sp3 hybrid orbitals. Secondary alcohols are easily oxidized without breaking carbon-carbon bonds only as far as the ketone stage. No further oxidation is seen except under very stringent conditions.Quality Control of 2,2′-Oxybis(ethan-1-ol)

Morphological evolution of 3D ZnO hierarchical nanostructures by diethylene glycol-assisted sol-gel synthesis for highly effective photocatalytic performance was written by Pham, Hoai Linh Linh;Nguyen, Van Hao;Nguyen, Van Khien;Tran, Nhu Hoa Thi;Le, Hong Phong Thi;Tran, Thi Huong;Nguyen, Hong Nhung;Lam, Kieu Giang Thi;Dang, Van Thanh. And the article was included in Journal of Sol-Gel Science and Technology in 2022.Quality Control of 2,2′-Oxybis(ethan-1-ol) This article mentions the following:

In this study, we focus on synthesizing various 3D ZnO hierarchical nanostructures (ZnH) for highly effective photocatalytic performance via an innovative sol-gel method using diethylene glycol as an assembly-guiding agent. The morphol. of 3D ZnH can be turned from nanospheres into nanoplate blocks and nanosheet-based flowers by increasing the concentration of diethylene glycol. Possible growth mechanisms are proposed for different assembly architectures. Anal. of characterization techniques reveal that the synthesized hierarchical structures exhibited a large sp. surface area, high degree of crystallinity, and a band gap in the range 2.95-3.11 eV, depending on their morphol. X-ray photoelectron and photoluminescence spectroscopy revealed the presence of rich oxygen vacancies introduced by the 3D ZnO hierarchical morphol. The photodegradation experiment results presented in ZnO nanosheet-based flower shown superior photoactivity of rhodamine B degradation compared with nanospheres and nanoplate blocks structures. This is attributed to the larger surface area, enhanced light absorption, and more effective photogenerated charge separation on account of their rich Vo. The establishment of relevant structural-optical property relationships is expected to provide deeper insights into the potential use of ZnH for innovative devices. Graphical abstract [graphic not available: see fulltext]. In the experiment, the researchers used many compounds, for example, 2,2′-Oxybis(ethan-1-ol) (cas: 111-46-6Quality Control of 2,2′-Oxybis(ethan-1-ol)).

2,2′-Oxybis(ethan-1-ol) (cas: 111-46-6) belongs to alcohols. Similar to water, an alcohol can be pictured as having an sp3 hybridized tetrahedral oxygen atom with nonbonding pairs of electrons occupying two of the four sp3 hybrid orbitals. Secondary alcohols are easily oxidized without breaking carbon-carbon bonds only as far as the ketone stage. No further oxidation is seen except under very stringent conditions.Quality Control of 2,2′-Oxybis(ethan-1-ol)

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Rafanelli, Claudio E. et al. published their research in Water, Air, and Soil Pollution in 1978 | CAS: 2451-01-6

rel-(1s,4s)-4-(2-Hydroxypropan-2-yl)-1-methylcyclohexanol hydrate (cas: 2451-01-6) belongs to alcohols. The oxygen atom of the strongly polarized O鈥旽 bond of an alcohol pulls electron density away from the hydrogen atom. This polarized hydrogen, which bears a partial positive charge, can form a hydrogen bond with a pair of nonbonding electrons on another oxygen atom. Converting an alcohol to an alkene requires removal of the hydroxyl group and a hydrogen atom on the neighbouring carbon atom. Dehydrations are most commonly carried out by warming the alcohol in the presence of a strong dehydrating acid, such as concentrated sulfuric acid.Name: rel-(1s,4s)-4-(2-Hydroxypropan-2-yl)-1-methylcyclohexanol hydrate

Photochlorination of organic substances by aqueous chloride ions codissolved with anionic NOx–. Part II. Effect of nitrite was written by Rafanelli, Claudio E.;Petriconi, Gianna L.;Papee, Henry M.. And the article was included in Water, Air, and Soil Pollution in 1978.Name: rel-(1s,4s)-4-(2-Hydroxypropan-2-yl)-1-methylcyclohexanol hydrate This article mentions the following:

Aqueous NO2– codissolved with Cl– promotes photochlorination of some reactive organic compounds in contact with those solutions Both overall patterns of the process and the quantum yields of this Cl transfer into the organic phase are very similar to the patterns and yields of reactions which involved NO3– and were carried out under artificial illumination. With analogy to those photoreactions of NO3–-Cl– systems, the overall kinetics outlined in the laboratory for systems comprising NO2– are also followed, with higher quantum yields, under sunlight illumination. In the experiment, the researchers used many compounds, for example, rel-(1s,4s)-4-(2-Hydroxypropan-2-yl)-1-methylcyclohexanol hydrate (cas: 2451-01-6Name: rel-(1s,4s)-4-(2-Hydroxypropan-2-yl)-1-methylcyclohexanol hydrate).

rel-(1s,4s)-4-(2-Hydroxypropan-2-yl)-1-methylcyclohexanol hydrate (cas: 2451-01-6) belongs to alcohols. The oxygen atom of the strongly polarized O鈥旽 bond of an alcohol pulls electron density away from the hydrogen atom. This polarized hydrogen, which bears a partial positive charge, can form a hydrogen bond with a pair of nonbonding electrons on another oxygen atom. Converting an alcohol to an alkene requires removal of the hydroxyl group and a hydrogen atom on the neighbouring carbon atom. Dehydrations are most commonly carried out by warming the alcohol in the presence of a strong dehydrating acid, such as concentrated sulfuric acid.Name: rel-(1s,4s)-4-(2-Hydroxypropan-2-yl)-1-methylcyclohexanol hydrate

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Escudero-Adan, Eduardo C. et al. published their research in Inorganic Chemistry in 2008 | CAS: 1122-71-0

6-Methyl-2-pyridinemethanol (cas: 1122-71-0) belongs to alcohols. Alcohols are among the most common organic compounds. They are used as sweeteners and in making perfumes, are valuable intermediates in the synthesis of other compounds, and are among the most abundantly produced organic chemicals in industry. A multistep synthesis may use Grignard-like reactions to form an alcohol with the desired carbon structure, followed by reactions to convert the hydroxyl group of the alcohol to the desired functionality.HPLC of Formula: 1122-71-0

Creation of a Nonsymmetric Dimethanolpyridine Ligand: A Rare Zn(salphen) Template Effect was written by Escudero-Adan, Eduardo C.;Benet-Buchholz, Jordi;Kleij, Arjan W.. And the article was included in Inorganic Chemistry in 2008.HPLC of Formula: 1122-71-0 This article mentions the following:

An interesting reversible, templated synthesis of unsym. pyridine-ligated Zn complexes was observed in solution and solid-state phases when Zn(salphen) complexes are reacted with MeOH-substituted pyridine substrates. The x-ray mol. structure of an unusual Zn3 supramol. assembly is reported, in which the central Zn atom is embedded in a distorted octahedral geometry and each of the single anionic O atoms of the pyridine groups coordinates to a Zn(salphen) unit. In the experiment, the researchers used many compounds, for example, 6-Methyl-2-pyridinemethanol (cas: 1122-71-0HPLC of Formula: 1122-71-0).

6-Methyl-2-pyridinemethanol (cas: 1122-71-0) belongs to alcohols. Alcohols are among the most common organic compounds. They are used as sweeteners and in making perfumes, are valuable intermediates in the synthesis of other compounds, and are among the most abundantly produced organic chemicals in industry. A multistep synthesis may use Grignard-like reactions to form an alcohol with the desired carbon structure, followed by reactions to convert the hydroxyl group of the alcohol to the desired functionality.HPLC of Formula: 1122-71-0

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Beiranvandi, Mojgan et al. published their research in Industrial Crops and Products in 2022 | CAS: 499-75-2

5-Isopropyl-2-methylphenol (cas: 499-75-2) belongs to alcohols. A strong base can deprotonate an alcohol to yield an alkoxide ion (R鈥昈鈭?. For example, sodamide (NaNH2), a very strong base, abstracts the hydrogen atom of an alcohol. Converting an alcohol to an alkene requires removal of the hydroxyl group and a hydrogen atom on the neighbouring carbon atom. Dehydrations are most commonly carried out by warming the alcohol in the presence of a strong dehydrating acid, such as concentrated sulfuric acid.Name: 5-Isopropyl-2-methylphenol

Biochar and super absorbent polymer improved growth, yield, and phytochemical characteristics of Satureja rechingeri Jamzad in water-deficiency conditions was written by Beiranvandi, Mojgan;Akbari, Nasser;Ahmadi, Abdolreza;Mumivand, Hasan;Nazarian, Farhad. And the article was included in Industrial Crops and Products in 2022.Name: 5-Isopropyl-2-methylphenol This article mentions the following:

Biochar is a stable, carbon-rich byproduct of organic matter thermal degradation The application of biochar demonstrates improved soil properties, water holding capacity, crop plant growth, and nutrient retention. The purpose of this study was to determine the effect of biochar and super absorbent on several phytochem. parameters of S. rechingeri Jamzad when grown in a water-stressed conditions. During two consecutive cropping seasons (2017-2019), an experiment was conducted using a split-plot factorial design with a randomized complete block design in three replications. Irrigation (100%, 80%, and 60% of irrigation requirement) [I] was used in the main plots, while subplots received a combination of two levels of cow manure biochar (0 and 10 t ha-1) [B] and two levels of stockosorb super absorbent (0 and 60 mg per plant) [SA]. Despite the relatively high diversity of compounds found in savory essential oils, the mean comparison revealed that IxBxSA had a significant effect on the majority of the primary components found in savory essential oils. Carvacrol (67.2-85%) was the first major constituent of savory essential oils in the two years, followed by 1, 8-cineole, terpinen-4-ol, 纬-terpinene, and linalool. The exptl. results indicated that drought stress increased the percentage of essential oil in two years but decreased dry matter and essential oil yield. Evidently, biochar and SA alone exhibit a similar effect on the content of savory essential oils, increasing growth rate and essential oil content (%). In general, this study confirmed that the combination of biochar and SA resulted in the highest savory leaf area, dry weight, and essential oil yield when compared to the application of biochar or SA alone under drought stress conditions. In the experiment, the researchers used many compounds, for example, 5-Isopropyl-2-methylphenol (cas: 499-75-2Name: 5-Isopropyl-2-methylphenol).

5-Isopropyl-2-methylphenol (cas: 499-75-2) belongs to alcohols. A strong base can deprotonate an alcohol to yield an alkoxide ion (R鈥昈鈭?. For example, sodamide (NaNH2), a very strong base, abstracts the hydrogen atom of an alcohol. Converting an alcohol to an alkene requires removal of the hydroxyl group and a hydrogen atom on the neighbouring carbon atom. Dehydrations are most commonly carried out by warming the alcohol in the presence of a strong dehydrating acid, such as concentrated sulfuric acid.Name: 5-Isopropyl-2-methylphenol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts