7699-76-5

Basic information

• Product Name: BenzeneMethaniMine,N-chloro-a-phenyl-
• Synonyms: BenzeneMethaniMine,N-chloro-a-phenyl-
• CAS NO: 7699-76-5
• Molecular Formula: C₁₃H₁₀ClN
• Molecular Weight: 215.6782
• Mol File: 7699-76-5.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 325.5°Cat760mmHg
• Flash Point: 150.6°C
• Appearance: /
• Density: 1.08g/cm³
• Vapor Pressure: 0.000436mmHg at 25°C
• Refractive Index: 1.567
• CAS DataBase Reference: BenzeneMethaniMine,N-chloro-a-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: BenzeneMethaniMine,N-chloro-a-phenyl-(7699-76-5)
• EPA Substance Registry System: BenzeneMethaniMine,N-chloro-a-phenyl-(7699-76-5)

Safety Data

• Hazardous Substances Data: 7699-76-5(Hazardous Substances Data)

Usage

Chemical compound

Benzenemethanimine, N-chloro-a-phenyl-

InChI:InChI=1/C13H10ClN/c14-15-13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10H

Upstream product

• 1013-88-3 Benzophenone imine 
• 100-47-0 benzonitrile 
• 34862-82-3 N,N-Dichlor-α-phenylbenzylamin 
• 91-00-9 Benzhydrylamine 
• 119-61-9 benzophenone 

Downstream Products

• 78488-69-4 N-(phenyldichloroseleno)diphenylketimine 
• 82388-29-2 N-(Diphenylmethylen)methansulfenamid 
• 82388-56-5 N-(Diphenylmethylen)ethansulfenamid 
• 41987-22-8 N-(diphenylmethylene)-S-phenylthiohydroxylamine 
• 82388-68-9 1,1-Diphenyl-N-thiocyanatomethanimin 
• 124842-07-5 <(diphenylmethylene)amino>triphenylphosphonium chloride 
• 93-98-1 N-phenyl benzoyl amide 
• 2866-82-2 N-(4-chlorophenyl)benzamide 
• 1461-22-9 tributyltin chloride 
• 119-61-9 benzophenone 

Relevant articles and documents

Rh(III)-catalyzed synthesis of isoquinolines using the N-Cl bond of N-chloroimines as an internal oxidant

The Rh(III)-catalyzed coupling of N-chloroimines with alkynes for the efficient synthesis of isoquinolines is reported. This represents the first use of the N-Cl bond of N-chloroimines as an internal oxidant for construction of the isoquinoline skeleton. The synthesis features atom and step economy, a green solvent (EtOH), mild reaction conditions, and a broad substrate scope.

An insight of the reactions of amines with trichloroisocyanuric acid

The reaction between amines or α-aminoacids with trichloroisocyanuric acid is studied under various conditions: N,N-dichloroamines, nitriles and ketones can be obtained from primary amines, while free aminoacids undergo oxidative decarboxylation to the corresponding nitrile of one less carbon atom.