212626-87-4

Basic information

• Product Name: 2-(2-bromophenyl)-2-ethylbutyronitrile
• Synonyms: 2-(2-bromophenyl)-2-ethylbutyronitrile
• CAS NO: 212626-87-4
• Molecular Weight: 252.154
• Mol File: 212626-87-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-(2-bromophenyl)-2-ethylbutyronitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-bromophenyl)-2-ethylbutyronitrile(212626-87-4)
• EPA Substance Registry System: 2-(2-bromophenyl)-2-ethylbutyronitrile(212626-87-4)

Safety Data

• Hazardous Substances Data: 212626-87-4(Hazardous Substances Data)

Upstream product

• 19472-74-3 2-(2-bromophenyl)acetonitrile 
• 75-03-6 ethyl iodide 

Downstream Products

• 212626-91-0 2-(2-bromophenyl)-2-ethylbutyraldehyde 
• 13312-96-4 2-ethyl-2-phenylbut-3-enenitrile 
• 929685-30-3 4-cyano-4-phenyl-hexanoic acid [2-(3,4-dimethoxy-phenyl)-ethyl]-methyl-amide 
• 929685-27-8 4-cyano-4-phenyl-hexanoic acid [2-(3,4-dimethoxy-phenyl)-ethyl]-amide 
• 212626-97-6 4-(2-bromophenyl)-4-ethylhex-2-enoic acid ethyl ester 
• 212627-02-6 4-(2-bromophenyl)4-ethylhexanoic acid ethyl ester 
• 1422149-01-6 N-acetyl-2-(2-bromophenyl)-2-ethylbutanamide 
• 1422148-72-8 2-(2-bromophenyl)-2-ethylbutanamide 

Relevant articles and documents

Copper-catalyzed domino coupling reaction: An efficient method to synthesize oxindoles

An efficient and novel procedure for a copper catalyzed domino coupling reaction has been developed, which afforded various oxindoles in good to excellent yields with tolerance of various substituents. In addition, this method could be applied to synthesize horsfiline and coerulescine in few steps with high total yields. The Royal Society of Chemistry 2012.

Synthesis of biphenyls mimicking the structure of the antimitotic rhazinilam

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