Benzyl alcohols

<p>Stability Moisture Sensitive<br>Applications 4-Chlorobenzyl Chloride is a benzylchloride derivative used in the preparation of various biologically active compounds such as bronchodilators and antibacterial agents.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Adams, M. et al.: Synth. Comm., 29, 2419 (1999); Foroumadi, A. et al.: Arch. Pharm. Res., 30, 138 (2007);<br></p>

<p>Applications Benzyl-2,3,4,5,6-D5 Alcohol is an isotopically labeled analog of Benzyl Alcohol (T536635), which is used in the synthesis of Cephalosporolide B as a versatile biomimetic synthetic precursor for chemical synthesis of other cephalosporides.<br>References Song, L. et al.: Org. Lett., 15, 5850 (2013);<br></p>

<p>3-Fluorophenol is a chemical compound that has a molecular formula of C6H3F3O and a molecular weight of 121.12. It has an intramolecular hydrogen bond between the hydroxyl group and the hydrogen atom in the 3-position, which is responsible for its stability. 3-Fluorophenol can be obtained by reacting 2-benzoylbenzoic acid with diazonium salt in water in the presence of sodium trifluoroacetate (NaC(O)CF3). The reaction mechanism involves an addition reaction between the diazonium salt and 2-benzoylbenzoic acid to form an intermediate, followed by nucleophilic attack from water on the intermediate to form an alcohol product. The kinetic energy of 3-fluorophenol is activated by hydrogen bonding, which leads to its ability to react with other molecules.</p>

<p>3-Aminobenzyl alcohol is a prodrug that is metabolized to 3-aminophenol, its active form. It has immunomodulatory properties and can be used to treat population growth. 3-Aminobenzyl alcohol binds to specific receptors on the surface of lymphocytes, which inhibits the immune system's response to foreign antigens. This drug also has photochemical properties and can be used as a photosensitizer in photodynamic therapy. 3-Aminobenzyl alcohol is a hydrogen bond acceptor with acidic functional groups and has been shown to bind with proteins through hydrogen bonding interactions. The hydrogen bond strength between the drug and protein depends on the pH of the solution, which may affect its efficacy in different cell types.</p>

<p>Synthetic building block; biomimetic anti-fungal</p>

<p>4-(Chloromethyl)benzyl alcohol is a colorless, water-soluble organic solvent that is used in polymerized and gel permeation chromatography. 4-(Chloromethyl)benzyl alcohol has been found to have antimicrobial properties against bacteria such as Pseudomonas aeruginosa, which can be attributed to its ability to cause the cross-linking of proteins. 4-(Chloromethyl)benzyl alcohol also has the ability to encapsulate drugs, making them more stable. This compound is not soluble in water and cannot be used as an antimicrobial agent for topical application. END&gt; END&gt; 6-Fluoro-3-indoxyl-beta-D-galactopyranoside is an antituberculosis drug that belongs to the class of rifamycins. It is the most active of the rifamycins for the treatment of tuberculosis. R</p>

<p>5-Amino-2-methoxyphenol is a p-hydroxybenzoic acid, which is an amide derivative of 5-amino-2-methoxybenzoic acid. It can be used to prepare a sample for the detection of fatty acids in human serum by cycle analysis. 5-Amino-2-methoxyphenol has been shown to have antinociceptive properties and can be used as a chemical precursor in the synthesis of other compounds. The reaction mechanism for 5-Amino-2-methoxyphenol has been determined using NMR spectroscopy and chemical structures. The compound is stable at neutral pH and reacts with hydrogen to form an intramolecular hydrogen bond between the hydroxyl group and the nitrogen atom on the amino group.</p>