316122-26-6

Basic information

• Product Name: N-((E)-4-phenylbut-3-en-2-ylidene)aniline
• Synonyms: N-((E)-4-phenylbut-3-en-2-ylidene)aniline
• CAS NO: 316122-26-6
• Molecular Weight: 221.302
• Mol File: 316122-26-6.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: N-((E)-4-phenylbut-3-en-2-ylidene)aniline(CAS DataBase Reference)
• NIST Chemistry Reference: N-((E)-4-phenylbut-3-en-2-ylidene)aniline(316122-26-6)
• EPA Substance Registry System: N-((E)-4-phenylbut-3-en-2-ylidene)aniline(316122-26-6)

Safety Data

• Hazardous Substances Data: 316122-26-6(Hazardous Substances Data)

Upstream product

• 953-21-9 N-phenylcinnamaldimine 
• 2181-44-4 trimethylsulfonium methylsulfate 
• 62-53-3 aniline 
• 122-57-6 1-Phenylbut-1-en-3-one 
• 1896-62-4 (E)-benzalacetone 
• 126404-68-0 Triphenyl-((1E,3E)-4-phenyl-2-phenylamino-buta-1,3-dienyl)-phosphonium; bromide 

Downstream Products

• 29475-88-5 trans-2-styrylindole 
• 1131890-58-8 (E)-1-phenyl-2-styryl-1H-indole 
• 1131890-63-5 (E)-5-methoxy-1-phenyl-2-styryl-1H-indole 
• 1131890-60-2 (E)-5-phenyl-6-styryl-5H-[1,3]dioxolo[4,5-f]indole 
• 1131890-62-4 (E)-6-(benzyloxy)-1-phenyl-2-styryl-1H-indole 
• 95121-84-9 (S)-(1-methyl-3-phenylallyl)phenylamine 
• 471930-02-6 (R)-(+)-N-(1-methyl-3-phenyl-2-propenyl)aniline 
• 128444-39-3 (E)-N-(4-phenylbut-3-en-2-yl)benzenamine 
• 13712-55-5 2,5-Dimethyl-1,3-diphenylpyrrole 

Relevant articles and documents

A Scalable Method for Regioselective 3-Acylation of 2-Substituted Indoles under Basic Conditions

Privileged structures such as 2-arylindoles are recurrent molecular scaffolds in bioactive molecules. We here present an operationally simple, high yielding and scalable method for regioselective 3-acylation of 2-substituted indoles under basic conditions

Conversion of (2-methyl-1-azabuta-1,3-diene)tricarbonyliron(0) complexes into (enamine)tricarbonyliron(0) complexes

Treatment of (2-methyl-1-azabuta-1,3-diene)tricarbonyliron(0) complexes with lithium diethylamide followed by a proton source leads to the formation of (enamine)tricarbonyliron(0) complexes in good yield.

TRIMETHYLSULFONIUM METHYLSULFATE, A SIMPLE AND EFFICIENT EPOXIDIZING AGENT.

Sulfonium salts 1 and 3 are highly reactive epoxidizing agents under phase transfer catalytic conditions.