Guan, Zhipeng et al. published their research in Angewandte Chemie, International Edition in 2021 | CAS: 106-21-8

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. The oxygen atom of the strongly polarized O―H 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. 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.COA of Formula: C10H22O

Electrochemical Oxidative Carbon-Atom Difunctionalization: Towards Multisubstituted Imino Sulfide Ethers was written by Guan, Zhipeng;Zhu, Shuxiang;Wang, Siyuan;Wang, Huamin;Wang, Siyuan;Zhong, Xingxing;Bu, Faxiang;Cong, Hengjiang;Lei, Aiwen. And the article was included in Angewandte Chemie, International Edition in 2021.COA of Formula: C10H22O The following contents are mentioned in the article:

Ethers (C-O/S) are ubiquitously found in a wide array of functional mols. and natural products. Nonetheless, the synthesis of imino sulfide ethers, containing an N(sp2)=C(sp2)-O/S fragment, still remains a challenge because of its sensitivity to acid. Developed here in is an unprecedented electrochem. oxidative carbon-atom difunctionalization of isocyanides, providing a series of novel multisubstituted imino sulfide ethers. Under metal-free and external oxidant-free conditions, isocyanides react smoothly with simple and readily available mercaptans and alcs. [e.g., 4-fluorobenzenethiol + Et isocyanoacetate + methanol → (Z)-I (80% isolated)]. Importantly, the procedure exhibited high stereoselectivities, excellent functional-group tolerance, and good efficiency on large-scale synthesis, as well as further derivatization of the products. This study involved multiple reactions and reactants, such as 3,7-Dimethyloctan-1-ol (cas: 106-21-8COA of Formula: C10H22O).

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. The oxygen atom of the strongly polarized O―H 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. 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.COA of Formula: C10H22O

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Qi, Rupeng et al. published their research in Angewandte Chemie, International Edition in 2022 | CAS: 367-93-1

(2R,3R,4S,5R,6S)-2-(Hydroxymethyl)-6-(isopropylthio)tetrahydro-2H-pyran-3,4,5-triol (cas: 367-93-1) 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. 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.Product Details of 367-93-1

Visible-light-promoted stereoselective C(sp3)-H glycosylation for the synthesis of C-glycoamino acids and C-glycopeptides was written by Qi, Rupeng;Wang, Chao;Ma, Zijian;Wang, Hongying;Chen, Qiao;Liu, Liangyu;Pan, Da;Ren, Xiaoyu;Wang, Rui;Xu, Zhaoqing. And the article was included in Angewandte Chemie, International Edition in 2022.Product Details of 367-93-1 The following contents are mentioned in the article:

The glycosylative modification of peptides could improve the pharmacol. properties of peptide drugs and deliver them efficiently to the target sites. Compared with O-/N-glycosides, C-glycosides exhibit more metabolic stability. We here disclose the first example of visible-light-promoted and Cu-catalyzed stereoselective C-glycosylation. The mild reaction conditions are compatible with various carbohydrate substrates, as demonstrated with a series of monosaccharides and a disaccharide, and are amenable to the synthesis of a wide variety of C-glycoamino acids and C-glycopeptidomimetics with good yields and excellent stereoselectivities. The dual-functional photocatalyst formed in situ via coordination of the glycine derivative and the chiral phosphine Cu complex could not only catalyze the photoredox process but also control the stereoselectivity of the glycosylation reaction. This study involved multiple reactions and reactants, such as (2R,3R,4S,5R,6S)-2-(Hydroxymethyl)-6-(isopropylthio)tetrahydro-2H-pyran-3,4,5-triol (cas: 367-93-1Product Details of 367-93-1).

(2R,3R,4S,5R,6S)-2-(Hydroxymethyl)-6-(isopropylthio)tetrahydro-2H-pyran-3,4,5-triol (cas: 367-93-1) 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. 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.Product Details of 367-93-1

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

En-nahli, Fatima et al. published their research in Rhazes: Green and Applied Chemistry in 2020 | CAS: 106-21-8

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. Under appropriate conditions, inorganic acids also react with alcohols to form esters. To form these esters, a wide variety of specialized reagents and conditions can be used. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.Application In Synthesis of 3,7-Dimethyloctan-1-ol

DFT study of the retention/release of odorant molecules in water using statistical methods was written by En-nahli, Fatima;Belhassan, Assia;Lakhlifi, Tahar;Bouachrine, Mohammed. And the article was included in Rhazes: Green and Applied Chemistry in 2020.Application In Synthesis of 3,7-Dimethyloctan-1-ol The following contents are mentioned in the article:

The D. Functional Theory (DFT) with Becke’s threeparameter hybrid functional using the LYP correlation functional (B3LYP/6-31G (d)), was employed in this work to calculate some quantum chem. descriptors of 51 odorant mols. (15 alcs., 11 aldehydes, 9 ketones, and 16 esters) with the Gaussian 09 software. A total of 37 mols. (2/3 of the data set) were placed in the formation set to construct the 2D-QSAR model, while the remaining 14 mols. (1/3 of the data set) constitute the test set. Statistical methods were used to link the quantum chem. descriptors with retention/release properties using multiple linear regression (MLR), the internal and external validation has been done to validate the model. The significant RLM model showed a good correlation between studied property and three mol. descriptors (EHomo, ET, Ea) with (R2=0.88; Q2=0.91 and R2pred=0.66) which is a good result. This study involved multiple reactions and reactants, such as 3,7-Dimethyloctan-1-ol (cas: 106-21-8Application In Synthesis of 3,7-Dimethyloctan-1-ol).

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. Under appropriate conditions, inorganic acids also react with alcohols to form esters. To form these esters, a wide variety of specialized reagents and conditions can be used. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.Application In Synthesis of 3,7-Dimethyloctan-1-ol

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Kundra, Milan et al. published their research in Industrial & Engineering Chemistry Research in 2021 | CAS: 106-21-8

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. Because alcohols are easily synthesized and easily transformed into other compounds, they serve as important intermediates in organic synthesis. 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.Electric Literature of C10H22O

Continuous Flow Hydrogenation of Flavorings and Fragrances Using 3D-Printed Catalytic Static Mixers was written by Kundra, Milan;Grall, Tom;Ng, Derrick;Xie, Zongli;Hornung, Christian H.. And the article was included in Industrial & Engineering Chemistry Research in 2021.Electric Literature of C10H22O The following contents are mentioned in the article:

A new type of additively manufactured catalytic static mixer, coated with alumina-supported metal catalysts, has been used for the hydrogenation of various model compounds commonly employed in the flavoring and fragrance industries. These heterogeneous catalytic reactions were performed inside an intensified tubular flow reactor housing several catalytic static mixers. In addition to electroplated and cold-sprayed catalyst coatings, which were presented by our group in earlier work, we herein demonstrate a series of alumina-supported metal catalysts for the first time, namely Pd, Pt, Ru, and Ni, supported on alumina and deposited on stainless-steel static mixers. The continuous flow hydrogenation of (-)-isopulegol at 24 bar and 130°C produced the high value product (-)-menthol at full conversion with a 98.8% purity and a space-time yield of 2.66 kg L-1 h-1. This study involved multiple reactions and reactants, such as 3,7-Dimethyloctan-1-ol (cas: 106-21-8Electric Literature of C10H22O).

3,7-Dimethyloctan-1-ol (cas: 106-21-8) belongs to alcohols. Because alcohols are easily synthesized and easily transformed into other compounds, they serve as important intermediates in organic synthesis. 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.Electric Literature of C10H22O

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Bachelier, Nicolas et al. published their research in Polyhedron in 1995 | CAS: 115-84-4

2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) belongs to alcohols. Because alcohols are easily synthesized and easily transformed into other compounds, they serve as important intermediates in organic synthesis. 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.HPLC of Formula: 115-84-4

Formation of neutral complexes of boric acid with 1,3-diols in organic solvents and in aqueous solution was written by Bachelier, Nicolas;Verchere, Jean-Francois. And the article was included in Polyhedron in 1995.HPLC of Formula: 115-84-4 The following contents are mentioned in the article:

From solubility measurements in organic media and extraction experiments, the values of the stability constants of neutral 1:1 complexes (HBL) formed between boric acid (HB) and 1,3-diols (L) were obtained in aqueous solution (Kcw) and in organic solvents (Kcs). The values of the partition coefficients of the diols (PL) and (PHBL) between H2O and the organic solvents also were calculated Generally, the addition of a diol to an aqueous solution of borax is accompanied by a decrease of pH due to the prevailing formation of borate species but, in the case of 2-methyl-2,4-pentanediol, the pH increased, in agreement with the formation of a single neutral complex. A modification of a previous potentiometric procedure yields simultaneously the values of the stability constants of the neutral and anionic complexes in aqueous solution This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4HPLC of Formula: 115-84-4).

2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) belongs to alcohols. Because alcohols are easily synthesized and easily transformed into other compounds, they serve as important intermediates in organic synthesis. 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.HPLC of Formula: 115-84-4

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Ebani, Patricia Regina et al. published their research in Journal of Molecular Structure in 2016 | CAS: 65-22-5

3-Hydroxy-5-(hydroxymethyl)-2-methylisonicotinaldehyde hydrochloride (cas: 65-22-5) 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. 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.Name: 3-Hydroxy-5-(hydroxymethyl)-2-methylisonicotinaldehyde hydrochloride

New manganese(II) and nickel(II) coordination compounds with N,O-polydentate ligands obtained from pyridoxal and tripodal units was written by Ebani, Patricia Regina;Fontana, Liniquer Andre;Campos, Patrick Teixeira;Rosso, Eduardo F.;Piquini, Paulo C.;Iglesias, Bernardo Almeida;Back, Davi Fernando. And the article was included in Journal of Molecular Structure in 2016.Name: 3-Hydroxy-5-(hydroxymethyl)-2-methylisonicotinaldehyde hydrochloride The following contents are mentioned in the article:

The authors have reported the synthesis involving the condensation of pyridoxal with tris(2-aminoethyl)amine obtained a tripodal ligand, as well as its subsequent complexation with the manganese(II) and nickel(II) ions. The structural anal. revealed, in the case of complex 1, the formation of a monomeric complex with Mn(II) species. In the complex 2, with Ni(II) metal ion, the authors describe the probable mechanism for the formation of hemiacetal in these complexes. Only the complex 1 catalyze the dismutation of superoxide efficiently with IC50 equal to 3.38 μM, evaluated through the nitro blue tetrazolium photoreduction inhibition superoxide dismutase assay, in aqueous solution of pH 7.8. D. functional theory calculations are done to characterize and compare the mol. frontier orbitals of the Mn(II) and Ni(II) complexes. This study involved multiple reactions and reactants, such as 3-Hydroxy-5-(hydroxymethyl)-2-methylisonicotinaldehyde hydrochloride (cas: 65-22-5Name: 3-Hydroxy-5-(hydroxymethyl)-2-methylisonicotinaldehyde hydrochloride).

3-Hydroxy-5-(hydroxymethyl)-2-methylisonicotinaldehyde hydrochloride (cas: 65-22-5) 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. 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.Name: 3-Hydroxy-5-(hydroxymethyl)-2-methylisonicotinaldehyde hydrochloride

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Castro, Juan M. et al. published their research in Scientific Reports in 2019 | CAS: 923-61-5

(2R)-3-(((2-Aminoethoxy)(hydroxy)phosphoryl)oxy)propane-1,2-diyl dipalmitate (cas: 923-61-5) belongs to alcohols. Under appropriate conditions, inorganic acids also react with alcohols to form esters. To form these esters, a wide variety of specialized reagents and conditions can be used. 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.Reference of 923-61-5

Budding and Division of Giant Vesicles Linked to Phospholipid Production was written by Castro, Juan M.;Sugiyama, Hironori;Toyota, Taro. And the article was included in Scientific Reports in 2019.Reference of 923-61-5 The following contents are mentioned in the article:

The self-reproduction of supramol. assemblies based on the synthesis and self-assembly of building blocks is a critical step towards the construction of chem. systems with autonomous, adaptive, and propagation properties. In this report, we demonstrate that giant vesicles can grow and produce daughter vesicles by synthesizing and incorporating phospholipids in situ from ad-hoc precursors. Our model involves acyl chain elongation via copper(I)-catalyzed azide-alkyne [3 + 2] cycloaddition reaction and the ensuing production of synthetic phospholipids to induce budding and division. In addition, the growth and budding of giant vesicles were compatible with the encapsulation and transfer of macromols. as large as lambda phage DNA to the buds. This chem. system provides a useful model towards the implementation of cell-like compartments capable of propagation and transport of biol. materials. This study involved multiple reactions and reactants, such as (2R)-3-(((2-Aminoethoxy)(hydroxy)phosphoryl)oxy)propane-1,2-diyl dipalmitate (cas: 923-61-5Reference of 923-61-5).

(2R)-3-(((2-Aminoethoxy)(hydroxy)phosphoryl)oxy)propane-1,2-diyl dipalmitate (cas: 923-61-5) belongs to alcohols. Under appropriate conditions, inorganic acids also react with alcohols to form esters. To form these esters, a wide variety of specialized reagents and conditions can be used. 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.Reference of 923-61-5

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Gabba, Matteo et al. published their research in Biophysical Journal in 2020 | CAS: 923-61-5

(2R)-3-(((2-Aminoethoxy)(hydroxy)phosphoryl)oxy)propane-1,2-diyl dipalmitate (cas: 923-61-5) 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. The most common reactions of alcohols can be classified as oxidation, dehydration, substitution, esterification, and reactions of alkoxides.Formula: C37H74NO8P

Weak Acid Permeation in Synthetic Lipid Vesicles and Across the Yeast Plasma Membrane was written by Gabba, Matteo;Frallicciardi, Jacopo;van ‘t Klooster, Joury;Henderson, Ryan;Syga, Lukasz;Mans, Robert;van Maris, Antonius J. A.;Poolman, Bert. And the article was included in Biophysical Journal in 2020.Formula: C37H74NO8P The following contents are mentioned in the article:

The authors present a fluorescence-based approach for determination of the permeability of small mols. across the membranes of lipid vesicles and living cells. With properly designed experiments, the method allows the authors to assess the membrane phys. properties both in vitro and in vivo. The permeability of weak acids increases in the order of benzoic > acetic > formic > lactic, both in synthetic lipid vesicles and the plasma membrane of Saccharomyces cerevisiae, but the permeability is much lower in yeast (one to two orders of magnitude). A relation between the mol. permeability and the saturation of the lipid acyl chain (i.e., lipid packing) in the synthetic lipid vesicles. were observed By analyzing wild-type yeast and a manifold knockout strain lacking all putative lactic acid transporters, the yeast plasma membrane is impermeable to lactic acid on timescales up to ∼2.5 h. This study involved multiple reactions and reactants, such as (2R)-3-(((2-Aminoethoxy)(hydroxy)phosphoryl)oxy)propane-1,2-diyl dipalmitate (cas: 923-61-5Formula: C37H74NO8P).

(2R)-3-(((2-Aminoethoxy)(hydroxy)phosphoryl)oxy)propane-1,2-diyl dipalmitate (cas: 923-61-5) 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. The most common reactions of alcohols can be classified as oxidation, dehydration, substitution, esterification, and reactions of alkoxides.Formula: C37H74NO8P

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Koroly, Joseph E. et al. published their research in Industrial and Engineering Chemistry in 1953 | CAS: 115-84-4

2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) belongs to alcohols. Under appropriate conditions, inorganic acids also react with alcohols to form esters. To form these esters, a wide variety of specialized reagents and conditions can be used. 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.Category: alcohols-buliding-blocks

Polymeric plasticizers. Preparation and characterization of a series of terminated polyesters was written by Koroly, Joseph E.;Beavers, Ellington M.. And the article was included in Industrial and Engineering Chemistry in 1953.Category: alcohols-buliding-blocks The following contents are mentioned in the article:

The general schematic structure for terminated polyesters L-G-(-A-G-)n-L, where A represents a dibasic acid, L a mono-basic acid, G a dihydric alc., and n is the number of repeating units, is the basis of preparation of a polymeric plasticizer series. The monobasic acid of the reported study is lauric; the dibasic acids are succinic, adipic, sebacic, glutaric, thiodipropionic, azelaic, and γ-methyl-γ-acetylpimelic; the glycols are 1,2-propylene, ethylene, trimethylene, 1,3-butylene, 2,2-dimethyl-1,3-propanediol, and 2-ethyl-2-butylpropanediol; and the values of n are 1-10. The rate and degree of completion of the first reaction stage, which was direct esterification, was characterized by determination of the acid number; and that of the second reaction stage, which was polymerization by trans-esterification, was characterized by melt viscosity of the reaction mixture 20 references. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Category: alcohols-buliding-blocks).

2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) belongs to alcohols. Under appropriate conditions, inorganic acids also react with alcohols to form esters. To form these esters, a wide variety of specialized reagents and conditions can be used. 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.Category: alcohols-buliding-blocks

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts

Huang, Qi et al. published their research in Spectrochimica Acta in 2016 | CAS: 65-22-5

3-Hydroxy-5-(hydroxymethyl)-2-methylisonicotinaldehyde hydrochloride (cas: 65-22-5) 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. 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 3-Hydroxy-5-(hydroxymethyl)-2-methylisonicotinaldehyde hydrochloride

A new “off-on” fluorescent probe for Al3+ in aqueous solution based on rhodamine B and its application to bioimaging was written by Huang, Qi;Zhang, Qingyou;Wang, Enze;Zhou, Yanmei;Qiao, Han;Pang, Lanfang;Yu, Fang. And the article was included in Spectrochimica Acta in 2016.Application In Synthesis of 3-Hydroxy-5-(hydroxymethyl)-2-methylisonicotinaldehyde hydrochloride The following contents are mentioned in the article:

In this paper, a new fluorescent probe has been synthesized and applied as “off-on” sensor for the detection of Al3+ with a high sensitivity and excellent selectivity in aqueous media. The sensor was easily prepared by one step reaction between rhodamine B hydrazide and pyridoxal hydrochloride named RBP. The structure of the sensor has been characterized by NMR and electron spray ionization-mass spectrometry. The fluorescence intensity and absorbance for the sensor showed a good linearity with the concentration of Al3+ in the range of 0-12.5 μM and 8-44 μM, resp., with detection limits of 0.23 μM and 1.90 μM. The sensor RBP was preliminarily applied to the determination of Al3+ in water samples from the lake of Henan University and tap water with satisfying results. Moreover, it can be used as a bioimaging reagent for imaging of Al3+ in living cells. This study involved multiple reactions and reactants, such as 3-Hydroxy-5-(hydroxymethyl)-2-methylisonicotinaldehyde hydrochloride (cas: 65-22-5Application In Synthesis of 3-Hydroxy-5-(hydroxymethyl)-2-methylisonicotinaldehyde hydrochloride).

3-Hydroxy-5-(hydroxymethyl)-2-methylisonicotinaldehyde hydrochloride (cas: 65-22-5) 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. 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 3-Hydroxy-5-(hydroxymethyl)-2-methylisonicotinaldehyde hydrochloride

Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts