7005-43-8

Basic information

• Product Name: 1,2-Benzenediol, 4-(phenylmethyl)- (9CI)
• Synonyms: 1,2-Benzenediol, 4-(phenylmethyl)- (9CI)
• CAS NO: 7005-43-8
• Molecular Formula: C₁₃H₁₂O₂
• Molecular Weight: 200.23318
• Product Categories: ALCOHOL
• Mol File: 7005-43-8.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,2-Benzenediol, 4-(phenylmethyl)- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-Benzenediol, 4-(phenylmethyl)- (9CI)(7005-43-8)
• EPA Substance Registry System: 1,2-Benzenediol, 4-(phenylmethyl)- (9CI)(7005-43-8)

Safety Data

• Hazardous Substances Data: 7005-43-8(Hazardous Substances Data)

Usage

Type of compound

Chemical compound

Derivative of

Resorcinol

Usage

Production of pharmaceuticals

Role in pharmaceuticals

Intermediate in the synthesis of medications for various medical conditions

Potential applications

Organic synthesis for the development of new compounds and materials

Safety concerns

May pose health risks and safety hazards if not used properly

Importance of handling

Careful handling is required to minimize risks and hazards

Upstream product

• 120-80-9 benzene-1,2-diol 
• 100-51-6 benzyl alcohol 
• 65-85-0 benzoic acid 
• 101-53-1 p-benzylphenol 
• 91-16-7 1,2-dimethoxybenzene 
• 98-88-4 benzoyl chloride 
• 4038-14-6 3,4-dimethoxybenzophenone 
• 7664-93-9 sulfuric acid 
• 71-43-2 benzene 
• 78238-97-8 (3,4-dimethoxyphenyl)phenylmethane 
• 100-44-7 benzyl chloride 

Downstream Products

• 68725-73-5 4',4''-Dibenzyl-2,3:11,12-dibenzo-18-krone-6 
• 90043-66-6 2,14-Dibenzyl-6,7,9,10,17,18,20,21-octahydro-5,8,11,16,19,22-hexaoxa-dibenzo[a,j]cyclooctadecene 
• 99-50-3 3,4-Dihydroxybenzoic acid 
• 65-85-0 benzoic acid 
• 688349-34-0 7-benzyl-3-methylene-3,4-dihydro-2H-benzo[b][1,4]dioxepine 

Relevant articles and documents

A template-free approach to nanotube-decorated polymer surfaces using 3,4-phenylenedioxythiophene (PhEDOT) monomers

In this work, novel 3,4-phenylenedioxythiophene (PhEDOT) monomers with alkyl, branched, and aromatic substituents were synthesized and tested for their efficacy at forming surfaces with unique wetting properties and surface morphology without the aid of surfactants. Monomers with a naphthalene substituent clearly showed the highest capacity to stabilize gas bubbles (O2 or H2) formed in solution during electrodeposition from trace water, resulting in the formation of nanotubes. Variation in the resulting density, diameter, and height of nanotubes was demonstrated by varying the electropolymerization protocol, conditions, or electrolyte used. The wetting induced by the nanotube formation results in the surfaces formed having both high contact angles with water (W) and strong adhesion, despite all polymers being intrinsically hydrophilic. This one-step and easily tunable approach to nanotube formation has potential to advance applications in membrane design, water transport and harvesting, as well as sensor design.

Conception, characterization and correlation of new marine odorants

Via a synthetic sequence consisting of PPA-mediated Friedel-Crafts acylation of veratrol (8), Clemmensen reduction, demethylation with TMSI, Williamson ether synthesis employing 3-chloro-2-(chloromethyl)prop-1-ene and in-situ ruthenium tetroxide oxidation, numerous substituted benzo[b][1,4]dioxepinones 15-27 and 2,3-dihydro-1H-5,9-di-oxacyclohepta[f]indenones 7, 13 and 14 were prepared to study their odor-structure correlation. In the course of these studies, we discovered the extremely powerful new marine odorant 7-(3′ -methylbutyl)benzo[b][1,4]dioxepin-3-one (16). On the basis of the measured odor threshold data, an olfactophore model was constructed that rationalizes the observed odor intensities, and indicates an aliphatic hydrophobe at a distance of 6.3 A from the centre of the aromatic-ring binding site. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003.

SYNTHESIS OF SUBSTITUTED AROMATIC AND CYCLOALIPHATIC DERIVATIVES OF 18-CROWN-6

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