41036-93-5

Basic information

• Product Name: Ethanone, 2-bromo-2-chloro-1-phenyl-
• Synonyms: 2-Brom-2-chlor-1-phenyl-aethanon;2-bromo-2-chloro-1-phenylethanone
• CAS NO: 41036-93-5
• Molecular Formula: C8H6BrClO
• Molecular Weight: 233.492
• Mol File: 41036-93-5.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Ethanone, 2-bromo-2-chloro-1-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 2-bromo-2-chloro-1-phenyl-(41036-93-5)
• EPA Substance Registry System: Ethanone, 2-bromo-2-chloro-1-phenyl-(41036-93-5)

Safety Data

• Hazardous Substances Data: 41036-93-5(Hazardous Substances Data)

Upstream product

• 532-27-4 1-chloroacetophenone 
• 70-11-1 α-bromoacetophenone 
• 74-97-5 chlorobromomethane 
• 6919-61-5 N-methoxy-N-methylbenzamide 
• 13665-04-8 2,2-dibromoacetophenone 
• 98-86-2 acetophenone 
• 93-58-3 benzoic acid methyl ester 

Downstream Products

• 91859-59-5 Anhydro-3-hydroxy-2-phenylthiazolo<3,2-c>quinazolin-4-ium hydroxyide 
• 124-48-1 chlorodibromomethane 
• 611-71-2 MANDELIC ACID 
• 65-85-0 benzoic acid 
• 1523497-70-2 C₈H₈BrClO 
• 1588767-33-2 C₈H₈BrClO 
• 91534-03-1 8-Oxo-9-phenyl-8H-pyrido[1,2-c]quinazoline-10,11-dicarboxylic acid dimethyl ester 
• 91534-00-8 C₂₁H₁₈N₂O₃S 
• 31327-17-0 (Z)-2-chloro-1-phenylvinyl diethyl phosphate 
• 67629-02-1 (Z)-2-chloro-1-phenylvinyl dimethyl phosphate 

Relevant articles and documents

Solvent-free preparation of α,α-dichloroketones with sulfuryl chloride

An efficient and facile method is reported for the synthesis of a series of α,α-dichloroketones. The direct dichlorination of methyl ketones and 1,3-dicarbonyls using an excess amount of sulfuryl chloride affords the corresponding gem-dichloro compounds in moderate to excellent yields. Moreover, the protocol features high yields, broad substrate scope, and simple reaction conditions without using any catalysts and solvents.

Facile Approach to Geminal HeterodihalogenationOne-Pot Synthesis of α-Bromo-α-Chloro Ketones

An efficient and practical protocol for the geminal heterodihalogenation of methyl ketones by using readily available dimethyl sulfoxide and a combination of HCl and HBr is reported. Control experiments suggested that the acidity of the solution, as well as the oxidizing ability and nucleophilicity of the dimethyl sulfoxide might work cooperatively in ensuring the success of the tandem substitution. Its operational simplicity, easy accessibility, and mild oxidative conditions suggest that the present strategy might be useful for the assembly of bromochloromethyl functional groups in drug discovery.

Laccase/TEMPO-mediated system for the thermodynamically disfavored oxidation of 2,2-dihalo-1-phenylethanol derivatives

An efficient methodology to oxidize β,β-dihalogenated secondary alcohols employing oxygen was achieved in a biphasic medium using the laccase from Trametes versicolor/TEMPO pair, providing the corresponding ketones in a clean fashion under very mild conditions. Moreover, a chemoenzymatic protocol has been applied successfully to deracemize 2,2-dichloro-1-phenylethanol combining this oxidation with an alcohol dehydrogenase-catalyzed bioreduction. the Partner Organisations 2014.