267651-22-9

Basic information

• Product Name: 1-(3-bromo-2-methoxyphenyl)ethanol
• Synonyms: 1-(3-bromo-2-methoxyphenyl)ethanol
• CAS NO: 267651-22-9
• Molecular Formula: C9H11BrO2
• Molecular Weight: 231.089
• EINECS: -0
• Mol File: 267651-22-9.mol

Chemical Properties

• CAS DataBase Reference: 1-(3-bromo-2-methoxyphenyl)ethanol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(3-bromo-2-methoxyphenyl)ethanol(267651-22-9)
• EPA Substance Registry System: 1-(3-bromo-2-methoxyphenyl)ethanol(267651-22-9)

Safety Data

• Hazardous Substances Data: 267651-22-9(Hazardous Substances Data)

Usage

Physical state

White solid

Solubility

Soluble in organic solvents

Melting point

94-96°C

Applications

a. Pharmaceutical and chemical synthesis processes
b. Reagent or intermediate in various chemical reactions
c. Production of materials such as polymers, coatings, and adhesives

Potential applications

a. Medicinal chemistry due to structural features
b. Possible biological activity

Suitability

a. For use in various industrial applications
b. Due to its properties, it can be used in the production of different materials

Upstream product

• 38603-09-7 2,6-dibromoanisole 
• 75-07-0 acetaldehyde 

Downstream Products

• 267651-28-5 (S)-3-[3-(3-Bromo-2-methoxy-phenyl)-2-((1S,2R)-2-phenyl-cyclohexyloxycarbonyloxy)-benzofuran-5-yl]-2-(2,2,2-trichloro-ethoxycarbonylamino)-propionic acid methyl ester 
• 267651-27-4 2(S)-(2,2,2-trichloroethoxycarbonylamino)-3-[3-(3-bromo-2-methoxyphenyl)-2-oxo-2,3-dihydrobenzofuran-5-yl]-propionic acid methyl ester 
• 267651-25-2 2(S)-(2,2,2-trichloroethoxycarbonylamino)-3-{4-[2-(3-bromo-2-methoxyphenyl)-2-oxo-ethoxy]-phenyl}-propionic acid methyl ester 
• 267651-26-3 2(S)-(2,2,2-trichloroethoxycarbonylamino)-3-[3-(3-bromo-2-methoxyphenyl)-benzofuran-5-yl]-propionic acid methyl ester 
• 267651-24-1 1-(3-bromo-2-methoxyphenyl)-2-chloroethanone 
• 267651-23-0 1-(3-bromo-2-methoxyphenyl)ethan-1-one 

Relevant articles and documents

A tyrosine-derived benzofuranone related to diazonamide A.

[formula: see text] Cyclization of 8 with PPA followed by MCPBA oxidation affords the benzofuranone 10. Treatment with a chiral chloroformate in the presence of DMAP affords the target benzofuranone 13 via an enol ester 12.