190965-43-6

Basic information

• Product Name: 2-BROMO-5-N-PROPYLOXYBENZOIC ACID
• Synonyms: 2-BROMO-5-N-PROPYLOXYBENZOIC ACID;2-BROMO-5-PROPOXYBENZOIC ACID
• CAS NO: 190965-43-6
• Molecular Formula: C₁₀H₁₁BrO₃
• Molecular Weight: 259.1
• Mol File: 190965-43-6.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-BROMO-5-N-PROPYLOXYBENZOIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 2-BROMO-5-N-PROPYLOXYBENZOIC ACID(190965-43-6)
• EPA Substance Registry System: 2-BROMO-5-N-PROPYLOXYBENZOIC ACID(190965-43-6)

Safety Data

• Hazardous Substances Data: 190965-43-6(Hazardous Substances Data)

Upstream product

• 2973-80-0 2-bromo-5-hydroxybenzaldehyde 
• 195005-37-9 2-bromo-5-propoxybenzaldehyde 

Downstream Products

• 913648-38-1 2-bromo-5-propoxy-benzoic acid methyl ester 
• 913648-48-3 1-benzo[1,3]-dioxol-5-yl-3-[4-methoxy-2-(2-methoxymethoxyethoxy)phenyl]-5-propoxy-1H-indene-2-carboxylic acid tert-butyl ester 
• 913648-42-7 (-)-(S)-2-(1-benzo[1,3]-dioxol-5-yl-2-tert-butoxy-carbonylethyl)-5-propoxy-benzoic acid methyl ester 
• 913648-40-5 2-(2-tert-butoxycarbonylvinyl)-5-propoxybenzoic acid methyl ester 

Relevant articles and documents

1,4-Addition of arylboronic acids to β-aryl-α,β-unsaturated ketones and esters catalyzed by a rhodium(I)-chiraphos complex for catalytic and enantioselective synthesis of selective endothelin A receptor antagonists

An enantioselective synthesis of acyclic β-diaryl ketones and esters via 1,4-addition of arylboronic acids to β-aryl-α,β-unsaturated ketones or esters is described. The complex in situ prepared from [Rh(nbd)2]BF4 and chiraphos was fo