39887-65-5

Basic information

• Product Name: Benzenecarboximidoyl chloride, 4-chloro-N-(phenylmethyl)-
• CAS NO: 39887-65-5
• Molecular Formula: C14H11Cl2N
• Molecular Weight: 264.154
• Mol File: 39887-65-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzenecarboximidoyl chloride, 4-chloro-N-(phenylmethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenecarboximidoyl chloride, 4-chloro-N-(phenylmethyl)-(39887-65-5)
• EPA Substance Registry System: Benzenecarboximidoyl chloride, 4-chloro-N-(phenylmethyl)-(39887-65-5)

Safety Data

• Hazardous Substances Data: 39887-65-5(Hazardous Substances Data)

Upstream product

• 7461-34-9 N-benzyl-p-chlorobenzamide 

Downstream Products

• 1609460-27-6 N-benzyl-4-chloro-N′-phenylbenzimidamide 
• 23982-86-7 1-benzyl-2-(4-chlorophenyl)-1H-benzo[d]imidazole 
• 1229610-04-1 2-(4-chloro-phenyl)-4-phenyl-quinazoline 
• 1218987-70-2 1-(tert-butylamino)-2-phenyl-4-p-chlorophenylpyrimido[6,1-a]isoquinolin-5-ium chloride 
• 1218987-73-5 1-(cyclohexylamino)-2-phenyl-4-p-chlorophenylpyrimido[6,1-a]isoquinolin-5-ium chloride 

Relevant articles and documents

Solvent/oxidant-switchable synthesis of multisubstituted quinazolines and benzimidazoles via metal-free selective oxidative annulation of arylamidines

A fast and simple divergent synthesis of multisubstituted quinazolines and benzimidazoles was developed from readily available amidines, via iodine(III)-promoted oxidative C(sp3)-C(sp2) and C(sp 2)-N bond formation in nonpolar and polar solvents, respectively. Further selective synthesis of quinazolines in polar solvent was realized by TEMPO-catalyzed sp3C-H/sp2C-H direct coupling of the amidine with K2S2O8 as the oxidant. No metal, base, or other additives were needed.

PROTOTROPIC MIGRATIONS IN THE PHOSPHORYLATION OF IMIDOYL CHLORIDES CONTAINING HYDROGEN ON THE N-α-CARBON ATOM. III. PHOSPHORYLATION OF SUBSTITUTED N-BENZYLBENZIMIDOYL CHLORIDES WITH TRIETHYL PHOSPHITE

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