90484-46-1

Basic information

• Product Name: 2-Propen-1-one, 2-bromo-1-phenyl- (9CI)
• Synonyms: 2-Propen-1-one, 2-bromo-1-phenyl- (9CI)
• CAS NO: 90484-46-1
• Molecular Formula: C₉H₇BrO
• Molecular Weight: 211.05528
• Product Categories: ACETYLHALIDE
• Mol File: 90484-46-1.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-Propen-1-one, 2-bromo-1-phenyl- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propen-1-one, 2-bromo-1-phenyl- (9CI)(90484-46-1)
• EPA Substance Registry System: 2-Propen-1-one, 2-bromo-1-phenyl- (9CI)(90484-46-1)

Safety Data

• Hazardous Substances Data: 90484-46-1(Hazardous Substances Data)

Upstream product

• 14088-57-4 2-diazo-1-phenyl-1-propanone 
• 1504-58-1 3-Phenyl-2-propyn-1-ol 
• 879-72-1 3-(dimethylamino)propiophenone hydrochloride 
• 51011-65-5 2,3-dibromo-1-phenylpropan-1-one 
• 4393-06-0 1-Phenyl-2-propen-1-ol 
• 768-03-6 Phenyl vinyl ketone 

Downstream Products

• 97427-58-2 methyl 4-bromo-5-oxo-2-bis(methoxycarbonyl)-5-phenylpentanoate 
• 97427-57-1 2-((Z)-2-Bromo-3-phenyl-3-trimethylsilanyloxy-allyl)-2-methoxycarbonyl-malonic acid dimethyl ester 

Relevant articles and documents

alpha-halogenated unsaturated aldehyde ketone preparation method

The invention relates to an alpha-halogenated unsaturated aldehyde ketone preparation method, which comprises: mixing a propargyl alcohol derivative, a halogen source, an acid and a solvent, and carrying out a heating reaction to obtain the alpha-halogena

Catalyst-Free Halogenation of α-Diazocarbonyl Compounds with N-Halosuccinimides: Synthesis of 3-Halooxindoles or Vinyl Halides

A novel catalyst-free halogenative cyclization of N-aryl diazoamides with N-halosuccinimides (NXS) is reported for the synthesis of 3-halooxindoles through a carbene-free mechanism. N-Aryl diazoamides reacted with NXS under mild and catalyst-free conditio

Preparation of α-haloacrylate derivatives via dimethyl sulfoxide-mediated selective dehydrohalogenation

(Chemical Equation Presented) Dimethyl sulfoxide causes α/β-dihalopropanoate derivatives to undergo efficient, selective dehydrohalogenation to form α-haloacrylate analogues. A variety of α-halo Michael acceptors were prepared in dimethyl sulfoxide under mild, base-free conditions, including the preparation of α-bromoacrolein and α-chloro- and bromoacrylonitriles. Synthesis of these molecules has been reported in the literature to be difficult. Among all the existing dehydrohalogenation procedures, this protocol is the most facile, practical, and environmentally benign process.