151287-95-5

Basic information

• Product Name: 3-methoxybenzyl acetate
• Synonyms: benzenemethanol, 3-methoxy-, acetate
• CAS NO: 151287-95-5
• Molecular Formula: C₁₀H₁₂O₃
• Molecular Weight: 180.2005
• Mol File: 151287-95-5.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 251°C at 760 mmHg
• Flash Point: 98.7°C
• Density: 1.083g/cm³
• Vapor Pressure: 0.021mmHg at 25°C
• Refractive Index: 1.499
• CAS DataBase Reference: 3-methoxybenzyl acetate(CAS DataBase Reference)
• NIST Chemistry Reference: 3-methoxybenzyl acetate(151287-95-5)
• EPA Substance Registry System: 3-methoxybenzyl acetate(151287-95-5)

Safety Data

• Hazardous Substances Data: 151287-95-5(Hazardous Substances Data)

Upstream product

• 13398-94-2 2-(3-hydroxyphenyl)ethanol 
• 141-78-6 ethyl acetate 
• 108-05-4 vinyl acetate 

Downstream Products

• 372523-17-6 3,5-dichloro-2-methoxybenzenesulfonic acid 3-[2-(3-allyloxy-4-cyanophenyl)ethoxy]-5-ethylphenyl ester 
• 372523-30-3 3,5-dichloro-2-methoxybenzenesulfonic acid 3-[2-(4-cyano-3-hydroxyphenyl)ethoxy]-5-ethylphenyl ester 
• 372523-16-5 2,3-dichlorobenzenesulfonic acid 3-[2-(3-allyloxy-4-cyanophenyl)ethoxy]-5-ethylphenyl ester 
• 372523-10-9 2,5-dichlorobenzenesulfonic acid 3-[2-(3-allyloxy-4-cyanophenyl)ethoxy]-5-methylphenyl ester 
• 372523-29-0 2,3-dichlorobenzenesulfonic acid 3-[2-(4-cyano-3-hydroxyphenyl)ethoxy]-5-ethylphenyl ester 
• 372523-05-2 2-methoxy-5-methylbenzenesulfonic acid 3-[2-(3-allyloxy-4-cyanophenyl)ethoxy]phenyl ester 
• 372522-92-4 2-allyloxy-4-(2-hydroxyethyl)benzonitrile 
• 372522-90-2 2-allyloxy-4-(2-hydroxyethyl)benzaldehyde 
• 372522-89-9 acetic acid 2-(4-formyl-3-hydroxyphenyl)ethyl ester 

Relevant articles and documents

SUBSTITUTED CYCLOPENTANES OR CYCLOPENTANONES AS THERAPEUTIC AGENTS

Therapeutic compounds, methods, and compositions are disclosed herein.

Statistical molecular design, parallel synthesis, and biological evaluation of a library of thrombin inhibitors

A library of thrombin inhibitors has been designed using statistical molecular design. An aromatic scaffold was used, with three varied positions corresponding to three pockets at the active site of thrombin (the S-, P-, and D-pockets). The selection was