Tag: 100-200

Salem, Mohamed Z. M. et al. published their research in International Biodeterioration & Biodegradation in 2016 | CAS: 2451-01-6

rel-(1s,4s)-4-(2-Hydroxypropan-2-yl)-1-methylcyclohexanol hydrate (cas: 2451-01-6) belongs to alcohols. Alkyl halides are often synthesized from alcohols, in effect substituting a halogen atom for the hydroxyl group. Under carefully controlled conditions, simple alcohols can undergo intermolecular dehydration to give ethers. This reaction is effective only with methanol, ethanol, and other simple primary alcohols.Recommanded Product: 2451-01-6

Evaluation of usage three natural extracts applied to three commercial wood species against five common molds was written by Salem, Mohamed Z. M.;Zidan, Yassin E.;El Hadidi, Nesrin M. N.;Mansour, Maisa M. A.;Abo Elgat, Wael A. A.. And the article was included in International Biodeterioration & Biodegradation in 2016.Recommanded Product: 2451-01-6 This article mentions the following:

Natural extracts have become of high interest in the past ten years for their inhibiting the growth of molds over wood and wood products surfaces in service or during the storage of building materials. In the present study, the antifungal effects of three natural extracts applied to three woods against five common molds were assessed. The growth of fungal hyphae of Alternaria alternata, Fusarium subglutinans, Chaetomium globosum, Aspergillus niger, and Trichoderma viride on the surfaces of Pinus sylvestris, Pinus rigida and Fagus sylvatica woods treated with extracts of Pinusrigida (heartwood), Eucalyptus camaldulensis (leaves) and Costus speciosus (rhizomes) was visually estimated GC/MS and FTIR analyses were used to identify the chem. constituents and the functional groups of extracts a-terpineol (24.91%), borneol (10.95%), terpin hydrate (9.60%), D-fenchyl alc. (5.99%), and limonene glycol (5.05%), which are the main constituents of P. rigida heartwood methanol extract The main chem. compounds of methanol extract from Eucalyptuscamaldulensis leaves were spathulenol (18.89%), cryptone (5.79%), 4,6,6-trimethyl-2-(3-methylbuta-1,3-dienyl)-3-oxatricyclo[5.1.0.0(2,4)]octane (5.79%), (3,3-dimethylcyclohexylidene)-(E)-acetaldehyde (5.57%), and ascaridole (4.32%). The main constituents identified in the distilled water extract from Costusspeciosus rhizomes were meso-erythritol (12.21%), methyl-2-methyl-1,3-oxothiolan-2-yl-ketone (11.61%), (all-Z)-5,8,11,14,17-eicosapentaenoic acid-Me ester (9.74%), diosgenin (5.07%), 2-ethyl-3-hydroxy-4H-pyran-4-one (4.43%), 3′,4′,7-trimethylquercetin (3.17%), and digitoxin (2.77%). Wood specimens treated at the level of 2% concentration of P. rigida heartwood extract observed good inhibition to the mold growth under laboratory conditions. These findings support the potential use of natural extracts for natural wood protection against mold infestation for surface treatment of wood. The results indicate that wood extracts may be useful for reducing the incidence of mold on wood products, but none of the materials evaluated completely inhibited the test fungi. These extracts may provide a useful value-added application for byproducts of lumber production from these species. In the experiment, the researchers used many compounds, for example, rel-(1s,4s)-4-(2-Hydroxypropan-2-yl)-1-methylcyclohexanol hydrate (cas: 2451-01-6Recommanded Product: 2451-01-6).

rel-(1s,4s)-4-(2-Hydroxypropan-2-yl)-1-methylcyclohexanol hydrate (cas: 2451-01-6) belongs to alcohols. Alkyl halides are often synthesized from alcohols, in effect substituting a halogen atom for the hydroxyl group. Under carefully controlled conditions, simple alcohols can undergo intermolecular dehydration to give ethers. This reaction is effective only with methanol, ethanol, and other simple primary alcohols.Recommanded Product: 2451-01-6

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Pal, Nabhendu et al. published their research in Dalton Transactions in 2019 | CAS: 29364-29-2

Sodium 2-methyl-2-propanethiolate (cas: 29364-29-2) belongs to alcohols. Alkyl halides are often synthesized from alcohols, in effect substituting a halogen atom for the hydroxyl group. 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.Recommanded Product: 29364-29-2

Transfer of hydrosulfide from thiols to iron(II): a convenient synthetic route to nonheme diiron(II)-hydrosulfide complexes was written by Pal, Nabhendu;Majumdar, Amit. And the article was included in Dalton Transactions in 2019.Recommanded Product: 29364-29-2 This article mentions the following:

While the attempted synthesis of diiron(II)-hydrosulfide complexes using HS– produced an insoluble precipitate, the reaction of Fe(BF4)2路6H2O, Et3N and HN-Et-HPTB with RSH (R = tBu, CH2Ph) yielded the desired complex, [Fe2(N-Et-HPTB)(SH)(H2O)](BF4)2 (1a). The synthesis, one electron oxidation and dioxygen activity of 1a in comparison with an analogous chloride complex, [Fe2(N-Et-HPTB)(Cl)(DMF)2](BF4)2 (2), are described. In the experiment, the researchers used many compounds, for example, Sodium 2-methyl-2-propanethiolate (cas: 29364-29-2Recommanded Product: 29364-29-2).

Sodium 2-methyl-2-propanethiolate (cas: 29364-29-2) belongs to alcohols. Alkyl halides are often synthesized from alcohols, in effect substituting a halogen atom for the hydroxyl group. 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.Recommanded Product: 29364-29-2

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Sampaolesi, Sofia et al. published their research in Food Chemistry: X in 2022 | CAS: 149-32-6

(2R,3S)-rel-Butane-1,2,3,4-tetraol (cas: 149-32-6) belongs to alcohols. Alkyl halides are often synthesized from alcohols, in effect substituting a halogen atom for the hydroxyl group. 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.Synthetic Route of C4H10O4

The synthesis of soluble and volatile bioactive compounds by selected brewer鈥瞫 yeasts: Antagonistic effect against enteropathogenic bacteria and food spoiler – toxigenic Aspergillus sp. was written by Sampaolesi, Sofia;Briand, Laura E.;De Antoni, Graciela;Leon Pelaez, Angela. And the article was included in Food Chemistry: X in 2022.Synthetic Route of C4H10O4 This article mentions the following:

Contamination by Aspergillus sp. and the accumulation of its mycotoxins in food and beverages have a high impact on human health and food safety. This investigation inquires the ability of brewer鈥瞫 yeasts discarded after fermentation (brewing fermentation residue, BFR) to synthesize bioactive compounds and to biocontrol Aspergillus sp. BFRs of Saccharomyces cerevisiae MBELGA62 and Pichia kudriavzevii MBELGA61 proved to have bacteriostatic properties and to be efficient in fungal growth reduction, decreasing the growth rate of Aspergillus flavus and Aspergillus parasiticus up to 37.8% and 42.5%, resp. Fungal mycelium degradation along with absentia of conidia was detected near the yeast inoculum. Moreover, the yeasts synthesize volatile bioactive compounds that extend Aspergillus sp. lag phase above 100% and decrease fungal growth rates from 20% towards 44%, along with the complete inhibition of conidia synthesis. These results indicate the potential of this residue to be used in biocontrol applications in the food industry. In the experiment, the researchers used many compounds, for example, (2R,3S)-rel-Butane-1,2,3,4-tetraol (cas: 149-32-6Synthetic Route of C4H10O4).

(2R,3S)-rel-Butane-1,2,3,4-tetraol (cas: 149-32-6) belongs to alcohols. Alkyl halides are often synthesized from alcohols, in effect substituting a halogen atom for the hydroxyl group. 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.Synthetic Route of C4H10O4

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Phumnok, Ekaroek et al. published their research in ACS Omega in 2022 | CAS: 111-46-6

2,2′-Oxybis(ethan-1-ol) (cas: 111-46-6) belongs to alcohols. Because alcohols are easily synthesized and easily transformed into other compounds, they serve as important intermediates in organic synthesis. 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 111-46-6

Preparation of Natural Rubber Composites with High Silica Contents Using a Wet Mixing Process was written by Phumnok, Ekaroek;Khongprom, Parinya;Ratanawilai, Sukritthira. And the article was included in ACS Omega in 2022.Application of 111-46-6 This article mentions the following:

A wet mixing process is proposed for filled rubber composites with a high silica loading to overcome the drawbacks of high energy consumption and workplace contamination of the conventional dry mixing process. Ball milling was adopted for preparing the silica dispersion because it has a simple structure, is easy to operate, and is a low-cost process that can be easily scaled up for industrial production The response surface methodol. was used to optimize the making of the silica dispersion. The optimum conditions for a well-dispersed silica suspension with the smallest silica particle size of 4.9 mm were an about 22% silica content and 62 h of ball milling. The effects of dry and wet mixing methods on the properties of silica-filled rubber composites were investigated in a broad range of silica levels from low to high loadings. The mixing method choice had little impact on the properties of rubber composites with low silica loadings. The silica-filled rubber demonstrated in this study, however, shows superior characteristics over the rubber composite prepared with conventional dry mixing, particularly with high silica loadings. When compared to silica-filled natural rubbers prepared by dry mixing (dry silica rubber, DSR), the wet mixing (for WSR) produced smaller silica aggregates with better dispersion. Due to the shorter heat history, the WSR exhibits superior curing characteristics such as a longer scorch time (2.2-3.3 min for WSR and 1.0-2.1 min for DSR) and curing time (4.1-4.5 min for WSR and 2.2-3.1 min for DSR). Addnl., the WSR has superior mech. properties (hardness, modulus, tensile strength, and especially the elongation at break (420-680% for WSR and 360-620% DSR)) over the DSR. The rolling resistance of WSR is lower than that of DSR. However, the reversed trend on the wet skid resistance is observed In the experiment, the researchers used many compounds, for example, 2,2′-Oxybis(ethan-1-ol) (cas: 111-46-6Application of 111-46-6).

2,2′-Oxybis(ethan-1-ol) (cas: 111-46-6) belongs to alcohols. Because alcohols are easily synthesized and easily transformed into other compounds, they serve as important intermediates in organic synthesis. 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 111-46-6

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Erigur, Esra Caner et al. published their research in Bioorganic & Medicinal Chemistry Letters in 2022 | CAS: 111-46-6

2,2′-Oxybis(ethan-1-ol) (cas: 111-46-6) 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. The most common reactions of alcohols can be classified as oxidation, dehydration, substitution, esterification, and reactions of alkoxides.Synthetic Route of C4H10O3

Design, synthesis and human carbonic anhydrase I, II, IX and XII inhibitory properties of 1,3-thiazole sulfonamides was written by Erigur, Esra Caner;Altug, Cevher;Angeli, Andrea;Supuran, Claudiu T.. And the article was included in Bioorganic & Medicinal Chemistry Letters in 2022.Synthetic Route of C4H10O3 This article mentions the following:

A series of novel 1,3-thiazole sulfonamides I [R = i-Pr, n-Bu, HOCH2CH2, Ph(CH2)4, etc.] has been designed, synthesized and studied their carbonic anhydrase (CA) inhibitory properties. The inhibition property of four human CA isoforms was investigated: hCA I, II, IX, and XII using the standard drug acetazolamide (AAZ) for comparison. The compounds I showed a wide range of inhibition potency towards the cytosolic enzyme hCA I. Nevertheless, the compounds I (R = n-Pr, i-Pr, HOCH2CHMe, HOCHMeCH2, MeOCH2CH2) have shown higher inhibition potential as compared to acetazolamide (KI = 250 nM). The abundant human cytosolic isoform, hCA II, was strongly inhibited by the most compounds in low nanomolar range (KI < 12.1 nM). On the other hand, almost all novel synthesized compounds have shown weaker inhibition potential as compared to acetazolamide against the tumor membrane- associated isoform hCA IX. Finally, the second tumor membrane-associated isoform, hCA XII, showed a wide range of potency that spanned from 9.3 to 729.6 nM. In the experiment, the researchers used many compounds, for example, 2,2′-Oxybis(ethan-1-ol) (cas: 111-46-6Synthetic Route of C4H10O3).

2,2′-Oxybis(ethan-1-ol) (cas: 111-46-6) 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. The most common reactions of alcohols can be classified as oxidation, dehydration, substitution, esterification, and reactions of alkoxides.Synthetic Route of C4H10O3

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Marzi, Elena et al. published their research in European Journal of Organic Chemistry in 2002 | CAS: 2968-93-6

2-(4-(Trifluoromethyl)phenyl)ethanol (cas: 2968-93-6) belongs to alcohols. Alkyl halides are often synthesized from alcohols, in effect substituting a halogen atom for the hydroxyl group. Under carefully controlled conditions, simple alcohols can undergo intermolecular dehydration to give ethers. This reaction is effective only with methanol, ethanol, and other simple primary alcohols.Computed Properties of C9H9F3O

Fluoro- or trifluoromethyl-substituted benzyl and phenethyl alcohols: Substrates for metal-mediated site-selective functionalization was written by Marzi, Elena;Spitaleri, Andrea;Mongin, Florence;Schlosser, Manfred. And the article was included in European Journal of Organic Chemistry in 2002.Computed Properties of C9H9F3O This article mentions the following:

It was possible to functionalize the three fluorobenzyl alcs. and the three 2-(fluorophenyl)ethanols by metalation and subsequent carboxylation, the prototype electrophilic trapping reaction. Triisopropylsilyl (TIPS) outperformed methoxymethyl (MOM) as an O-protective group making seven new fluorobenzoic acids, including I and II, accessible in 63% average yield. The TIPS group tolerates weakly basic and acidic media and may facilitate further structural elaboration. The unprotected alcs. reacted more sluggishly and were unable to provide two of the targeted products. The yield averaged only 46% in the five other cases. The direct metalation of fluorinated benzyl and phenethyl alcs. remains nevertheless an attractive option because of its operational simplicity. All three (trifluoromethyl)benzyl alcs. and two of the three (trifluoromethyl)phenethyl alc. isomers were successfully submitted to the metalation/functionalization sequence. These five starting materials gave rise to a total nine new benzoic acids or lactones, e.g. III. Despite the poor yields (31% on average), the employed organometallic methods are extremely regioselective, economical and easy to perform. In the experiment, the researchers used many compounds, for example, 2-(4-(Trifluoromethyl)phenyl)ethanol (cas: 2968-93-6Computed Properties of C9H9F3O).

2-(4-(Trifluoromethyl)phenyl)ethanol (cas: 2968-93-6) belongs to alcohols. Alkyl halides are often synthesized from alcohols, in effect substituting a halogen atom for the hydroxyl group. Under carefully controlled conditions, simple alcohols can undergo intermolecular dehydration to give ethers. This reaction is effective only with methanol, ethanol, and other simple primary alcohols.Computed Properties of C9H9F3O

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Mersich-Vetsey-Kormendi, Agnes et al. published their research in Gyogyszereszet in 1972 | CAS: 2451-01-6

rel-(1s,4s)-4-(2-Hydroxypropan-2-yl)-1-methylcyclohexanol hydrate (cas: 2451-01-6) 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. 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.Electric Literature of C10H22O3

Changes of the particle size in suspension type medicines was written by Mersich-Vetsey-Kormendi, Agnes. And the article was included in Gyogyszereszet in 1972.Electric Literature of C10H22O3 This article mentions the following:

Medicinal suspensions containing terpine hydrate, norcaine, salicylamide, Bi salicylate in aqueous medium, norcaine, Na salicylate, amidopyrine, caffeine and Na benzoate, phenobarbital and Na noramidopyrine methanesulfonate in soft or solid fatty medium were examined for stability based on the initial parameters. No generalization could be made, hence the elaboration of new formulations of medicinal suspensions, the optimum conditions should be determined individually. In the experiment, the researchers used many compounds, for example, rel-(1s,4s)-4-(2-Hydroxypropan-2-yl)-1-methylcyclohexanol hydrate (cas: 2451-01-6Electric Literature of C10H22O3).

rel-(1s,4s)-4-(2-Hydroxypropan-2-yl)-1-methylcyclohexanol hydrate (cas: 2451-01-6) 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. 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.Electric Literature of C10H22O3

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Rout, P. K. et al. published their research in Fafai Journal in 2001 | CAS: 2451-01-6

rel-(1s,4s)-4-(2-Hydroxypropan-2-yl)-1-methylcyclohexanol hydrate (cas: 2451-01-6) 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. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.Safety of rel-(1s,4s)-4-(2-Hydroxypropan-2-yl)-1-methylcyclohexanol hydrate

Fractional hydrodistillation of Citronella (Cymbopogon winterianus Jowitt) was written by Rout, P. K.;Jena, K. S.;Rao, Y. R.. And the article was included in Fafai Journal in 2001.Safety of rel-(1s,4s)-4-(2-Hydroxypropan-2-yl)-1-methylcyclohexanol hydrate This article mentions the following:

Fractional hydro-distillation of Citronella Grass (C. winterianus Jowitt) and anal. of the decanted oil fractions showed that citronellal-rich fractions and sesquiterpenoid-rich fractions can be separated at the hydrodistillation stage itself. About 6% essential oil is lost in the aqueous layer. Further, 4 constituents, 6-methyl-5-hepten-2-one, benzyl alc., 2-[2-hydroxy-2-propyl]-5-menthylcyclohexanol and terpin hydrate present in significant quantities in the aqueous layer are not detected in any of the decanted oil fractions. In the experiment, the researchers used many compounds, for example, rel-(1s,4s)-4-(2-Hydroxypropan-2-yl)-1-methylcyclohexanol hydrate (cas: 2451-01-6Safety of 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. 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. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.Safety of rel-(1s,4s)-4-(2-Hydroxypropan-2-yl)-1-methylcyclohexanol hydrate

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Fache, Fabienne et al. published their research in Tetrahedron Letters in 1995 | CAS: 94022-96-5

2-(Trifluoromethyl)phenethyl alcohol (cas: 94022-96-5) belongs to alcohols. Alkyl halides are often synthesized from alcohols, in effect substituting a halogen atom for the hydroxyl group. Under carefully controlled conditions, simple alcohols can undergo intermolecular dehydration to give ethers. This reaction is effective only with methanol, ethanol, and other simple primary alcohols.Application In Synthesis of 2-(Trifluoromethyl)phenethyl alcohol

A catalytic stereo- and chemo-selective method for the reduction of substituted aromatics was written by Fache, Fabienne;Lehuede, Stephan;Lemaire, Marc. And the article was included in Tetrahedron Letters in 1995.Application In Synthesis of 2-(Trifluoromethyl)phenethyl alcohol This article mentions the following:

Various substituted aromatics have been reduced using colloidal ruthenium under H2 pressure with good stereoselectivity (cis/trans up to 60). Interesting chemoselectivities are also observed In the experiment, the researchers used many compounds, for example, 2-(Trifluoromethyl)phenethyl alcohol (cas: 94022-96-5Application In Synthesis of 2-(Trifluoromethyl)phenethyl alcohol).

2-(Trifluoromethyl)phenethyl alcohol (cas: 94022-96-5) belongs to alcohols. Alkyl halides are often synthesized from alcohols, in effect substituting a halogen atom for the hydroxyl group. Under carefully controlled conditions, simple alcohols can undergo intermolecular dehydration to give ethers. This reaction is effective only with methanol, ethanol, and other simple primary alcohols.Application In Synthesis of 2-(Trifluoromethyl)phenethyl alcohol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Li, Zhe et al. published their research in Journal of Thermal Analysis and Calorimetry in 2022 | CAS: 499-75-2

5-Isopropyl-2-methylphenol (cas: 499-75-2) belongs to alcohols. Alkyl halides are often synthesized from alcohols, in effect substituting a halogen atom for the hydroxyl group. 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.Formula: C10H14O

New insights into the thermal degradation behavior of Hydroxypropyl-beta-cyclodextrin inclusion complexes containing carvacrol essential oil via thermogravimetric analysis was written by Li, Zhe;Jiang, Xiaoxia;Zhu, Lin;Chen, Fucai;Liu, Hongning;Ming, Liangshan. And the article was included in Journal of Thermal Analysis and Calorimetry in 2022.Formula: C10H14O This article mentions the following:

The physicochem. properties and thermodn. parameters of cyclodextrin inclusion complexes (ICs) containing essential oil were investigated by thermogravimetric anal. It is necessary to understand the ICs thermal decomposition behavior and kinetics to control and elucidate the inclusion complexation mechanisms. Carvacrol essential oil was encapsulated with hydroxypropyl-beta-cyclodextrin (HP-尾 CD) using the freeze-drying method. The IC was characterized by SEM, FT-IR, and phase solubility, which confirmed that there were mol. interactions between the carvacrol essential oil and HP-尾 CD. Moreover, thermal experiments were carried out by a thermogravimetric analyzer at different heating rates (10-40 掳C min-1). In addition, three different models, i.e., FOW, KAS, and Starink, were used to calculate the kinetic energy. The FOW was a more proficient model for the calculation of activation energy (Ea). Further, the average values of Ea varied from conversion, and for carvacrol, HP-尾 CD, and carvacrol/HP-尾 CD IC, they were found to be 70.56, 162.15, and 152.57 kJ mol-1 based on the FOW model, resp. In general, carvacrol encapsulated into HP-尾 CD as an IC showed high thermal stability. The kinetic results could be useful in predicting the thermal performance of IC and in helping optimize exptl. procedures for the encapsulation of essential oils in cyclodextrins. In the experiment, the researchers used many compounds, for example, 5-Isopropyl-2-methylphenol (cas: 499-75-2Formula: C10H14O).

5-Isopropyl-2-methylphenol (cas: 499-75-2) belongs to alcohols. Alkyl halides are often synthesized from alcohols, in effect substituting a halogen atom for the hydroxyl group. 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.Formula: C10H14O

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts