35151-93-0

Basic information

• Product Name: Benzenemethanol, 2-hydroxy-6-pentadecyl-
• Synonyms: 2-Hydroxymethyl-tetrahydrocardanol;2-hydroxymethyl-3-pentadecylphenol;anacardic alcohol;2-Hydroxy-6-pentadecyl-benzylalkohol;2-hydroxy-6-pentadecylbenzyl alcohol;Benzenemethanol,2-hydroxy-6-pentadecyl
• CAS NO: 35151-93-0
• Molecular Formula: C22H38O2
• Molecular Weight: 334.53600
• Mol File: 35151-93-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzenemethanol, 2-hydroxy-6-pentadecyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanol, 2-hydroxy-6-pentadecyl-(35151-93-0)
• EPA Substance Registry System: Benzenemethanol, 2-hydroxy-6-pentadecyl-(35151-93-0)

Safety Data

• Hazardous Substances Data: 35151-93-0(Hazardous Substances Data)

Upstream product

• 485386-80-9 ethyl 2-methoxy-6-pentadecylbenzoate 
• 79688-35-0 anacardic anhydride 
• 38449-27-3 6-pentadecylsalicylic acid methyl ester 
• 79688-39-4 8-pentadecyl-1-oxaspiro<2.5>octa-5,7-dien-4-one 
• 79688-37-2 anacardaldehyde 
• 16611-84-0 6-Pentadecylsalicylic Acid 

Downstream Products

• 79688-37-2 anacardaldehyde 
• 79688-40-7 (2-methoxy-6-(pentadecyl)phenyl)methanol 
• 79688-41-8 anacardic alcohol dimethyl ether 
• 637009-61-1 2-methoxy-6-pentadecylbenzaldehyde 

Relevant articles and documents

Design, synthesis and biological evaluation of benzimidazole/benzothiazole and benzoxazole derivatives as cyclooxygenase inhibitors

We have synthesised a series of 2-[[2-alkoxy-6-pentadecylphenyl)methyl]thio]-1H-benzimidazoles/benzothiazoles and benzoxazoles from anacardic acid and investigated their ability to inhibit human cyclooxygenase-2 enzyme (COX-2). The active compounds were s

The separation and synthesis of lipidic 1,2- and 1,3-diols from natural phenolic lipids for the complexation and recovery of boron

A study has been made of the semi-synthesis of 1,3-diols (anacardic alcohols) from natural phenolic lipid resources from Anacardium occidentale and Anacardium giganteum which have given C15 and C11 derivatives, respectively. An isomeric 1,3-diol (isoanacardic alcohol) has been obtained from cardanol separated from technical cashew nut-shell liquid. Homologous1,3-diols have been synthesised from a range of synthetic 2-alkyl-, 3-alkyl- and 4-alkylphenols and from 6-alkylsalicylic acids. The natural 1,2-diol, urushiol, from Rhus vernicifera has been purified. All these lipidic compounds have been studied for their complexation and the potential recovery of boron as boric acid.