860243-44-3

Basic information

• Product Name: 4-bromo-2-chloro-3-hydroxy-benzaldehyde
• Synonyms: 4-bromo-2-chloro-3-hydroxy-benzaldehyde
• CAS NO: 860243-44-3
• Molecular Weight: 235.465
• Mol File: 860243-44-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 4-bromo-2-chloro-3-hydroxy-benzaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 4-bromo-2-chloro-3-hydroxy-benzaldehyde(860243-44-3)
• EPA Substance Registry System: 4-bromo-2-chloro-3-hydroxy-benzaldehyde(860243-44-3)

Safety Data

• Hazardous Substances Data: 860243-44-3(Hazardous Substances Data)

Upstream product

• 56962-10-8 2-chloro-3-hydroxybenzaldehyde 
• 100-83-4 meta-hydroxybenzaldehyde 
• 1207343-84-7 2-chloro-3-dimethoxymethyl phenol 
• 67-66-3 chloroform 
• 7726-95-6 bromine 

Downstream Products

• 860590-39-2 4-bromo-2-chloro-3-hydroxy-benzyl alcohol 
• 91658-95-6 4-bromo-2-chloro-3-hydroxy-benzoic acid 
• 1207343-85-8 6-bromo-2-chloro-3-dimethoxymethyl phenol 
• 1207343-86-9 3-chloro-4-dimethoxymethyl-2-hydroxybenzoic acid methyl ester 
• 1207343-87-0 3-chloro-4-dimethoxymethyl-2-trifluoromethanesulfonyloxybenzoic acid methyl ester 
• 1207343-88-1 3-chloro-4-dimethoxymethyl-2-(1-oxothianylideneamino)benzoic acid methyl ester 
• 1207343-90-5 3-chloro-4-formyl-2-(1-oxothianylidene amino)benzoic acid methyl ester 
• 1207343-91-6 [3-chloro-4-dimethoxymethyl-2-(1-oxothianylideneamino)phenyl]methanol 
• 1207343-92-7 (2-chloro-3-dimethoxymethyl-6-methoxymethylphenyl)-(1-oxothianylidene)amine 
• 1207343-93-8 4-bromo-2-chloro-3-hydroxybenzoic acid methyl ester 
• 1207344-03-3 4-bromo-2-chloro-3-methoxybenzoic acid methyl ester 
• 1207343-94-9 2-chloro-4-cyano-3-methoxybenzoic acid methyl ester 
• 1207343-95-0 2-chloro-4-cyano-3-hydroxybenzoic acid methyl ester 
• 1207343-89-2 2-chloro-3-(1-oxothianylideneamino)terephthalic acid 4-methyl ester 

Relevant articles and documents

Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and Applications

An ortho-selective ammonium chloride salt-catalyzed direct C-H monohalogenation of phenols and 1,1′-bi-2-naphthol (BINOL) with 1,3-dichloro-5,5-dimethylhydantoin (DCDMH) as the chlorinating agent has been developed. The catalyst loading was low (down to 0.01 mol %) and the reaction conditions were very mild. A wide range of substrates including BINOLs were compatible with this catalytic protocol. Chlorinated BINOLs are useful synthons for the synthesis of a wide range of unsymmetrical 3-aryl BINOLs that are not easily accessible. In addition, the same catalytic system can facilitate the ortho-selective selenylation of phenols.