620-24-6 | 3-Hydroxybenzyl alcohol

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$6.00	$4.00
5g	≥98%	in stock	$19.00	$13.00
10g	97%	in stock	$22.00	$16.00
25g	98%	in stock	$50.00	$35.00
100g	≥98%	in stock	$118.00	$82.00
500g	≥98%	in stock	$579.00	$405.00

Description

• Catalog Number: AB65123
• Chemical Name: 3-Hydroxybenzyl alcohol
• CAS Number: 620-24-6
• Molecular Formula: C7H8O2
• Molecular Weight: 124.1372
• MDL Number: MFCD00004643
• SMILES: OCc1cccc(c1)O
• NSC Number: 60735

Computed Properties

• Complexity: 83
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 9
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 1
• XLogP3: 0.5

Literature

• Biosynthesis and toxicological effects of patulin.

  Toxins 20100401

• Structure-toxicity relationship of phenolic analogs as anti-melanoma agents: an enzyme directed prodrug approach.

  Chemico-biological interactions 20100212

• Experimental stroke protection induced by 4-hydroxybenzyl alcohol is cancelled by bacitracin.

  Neuroscience research 20090601

• Molecular cloning and functional characterization of two CYP619 cytochrome P450s involved in biosynthesis of patulin in Aspergillus clavatus.

  Microbiology (Reading, England) 20090501

• Reactions of tertiary phosphines with alcohols in aqueous media.

  Inorganic chemistry 20090105

• Synthesis and in vivo evaluation of [O-methyl-11C](2R,4R)-4-hydroxy-2-[2-[2-[2-(3-methoxy)phenyl]ethyl]phenoxy]ethyl-1-methylpyrrolidine as a 5-HT2A receptor PET ligand.

  Nuclear medicine and biology 20060501

• Positive homotropic allosteric binding of benzenediols in a hydrindacene-based exoditopic receptor: cooperativity in amide hydrogen bonding.

  Journal of the American Chemical Society 20040428

• Screening for metabolites from Penicillium novae-zeelandiae displaying radical-scavenging activity and oxidative mutagenicity: isolation of gentisyl alcohol.

  Mutation research 20030805

• In vitro metabolism of a nitroderivative of acetylsalicylic acid (NCX4016) by rat liver: LC and LC-MS studies.

  Journal of pharmaceutical and biomedical analysis 20020801

• P-cresol and 3,5-xylenol methylhydroxylases in Pseudomonas putida N.C.I.B. 9896.

  The Biochemical journal 19781101

• The aromatic alcohol dehydrogenases in Pseudomonas putida N.C.I.B. 9869 grown on 3,5-xylenol and p-cresol.

  The Biochemical journal 19781101