39887-72-4

Basic information

• Product Name: N-allylbenzimidoyl chloride
• Synonyms: N-allylbenzimidoyl chloride
• CAS NO: 39887-72-4
• Molecular Weight: 179.649
• Mol File: 39887-72-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N-allylbenzimidoyl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: N-allylbenzimidoyl chloride(39887-72-4)
• EPA Substance Registry System: N-allylbenzimidoyl chloride(39887-72-4)

Safety Data

• Hazardous Substances Data: 39887-72-4(Hazardous Substances Data)

Upstream product

• 98-88-4 benzoyl chloride 
• 10283-95-1 N-allylbenzamide 
• 65-85-0 benzoic acid 

Downstream Products

• 80784-92-5 N-Allyl-N'-[4-(2-diisopropylamino-ethoxy)-phenyl]-benzamidine 
• 79507-99-6 1-{[(Z)-Allylimino]-phenyl-methyl}-5-methyl-1H-pyrazole-3-carboxylic acid methyl ester 
• 1262150-91-3 C₂₇H₂₇N 
• 1439357-03-5 methyl 1-allyl-7-fluoro-4-oxo-2-phenyl-1,4-dihydroquinoline-3-carboxylate 
• 66275-62-5 5-methyl-2-phenyl-1-(p-tolyl)-1H-imidazole 
• 55981-81-2 5-methyl-1,2-diphenyl-1H-imidazole 
• 68674-67-9 4-ethyl-2-phenylquinazoline 

Relevant articles and documents

Divergent Synthesis of Imidazoles and Quinazolines via Pd(OAc)2-Catalyzed Annulation of N-Allylamidines

A Pd(OAc)2-catalyzed divergent synthesis of multisubstituted imidazoles and quinazolines from N-allylamidines has been developed. In the presence of oxidant O2 from air and/or a ligand and Pd(OAc)2, imidazoles were obtaine

Transition metal-free one-pot synthesis of 2-substituted 3-carboxy-4-quinolone and chromone derivatives

A novel one-pot synthesis of the 2-substituted 3-carboxy-4-quinolone/ chromone derivatives from readily available 3-oxo-3-arylpropanoates and amides/acyl chlorides is reported, without any transition metal aid. The Royal Society of Chemistry 2013.