81512-13-2

Basic information

• Product Name: Benzenamine, 3-chloro-N-(1-phenylethylidene)-
• CAS NO: 81512-13-2
• Molecular Formula: C14H12ClN
• Molecular Weight: 229.709
• Mol File: 81512-13-2.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: Benzenamine, 3-chloro-N-(1-phenylethylidene)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, 3-chloro-N-(1-phenylethylidene)-(81512-13-2)
• EPA Substance Registry System: Benzenamine, 3-chloro-N-(1-phenylethylidene)-(81512-13-2)

Safety Data

• Hazardous Substances Data: 81512-13-2(Hazardous Substances Data)

Upstream product

• 98-86-2 acetophenone 
• 108-42-9 3-chloro-aniline 
• 20102-12-9 2-hydroxy-2-phenylpropionitrile 
• 536-74-3 phenylacetylene 
• 81512-05-2 2-((3-chlorophenyl)amino)-2-phenylpropanenitrile 

Downstream Products

• 1609488-36-9 (S)-3-chloro-N-(1-phenylethyl)aniline 
• 109240-37-1 (R)-3-chloro-N-(1-phenylethyl)aniline 
• 109240-37-1 N-α-phenylethyl-m-chloroaniline 

Relevant articles and documents

Synthesis of Schiff bases of acetophenone with aniline and its different chloro-substituted derivatives, and study of their antioxidant, enzyme inhibitory and antimicrobial properties

In the present work, five different Schiff bases of acetophenone were synthesized with aniline (AL1) and its mono- and di-chloro derivatives including ortho-chloroaniline (AL2), meta-chloroaniline (AL3), para-chloroaniline (AL4), and 2,4-dichloroaniline (

Synthesis of group 4 metal complexes stabilized by an amine-bridged bis(phenolato) ligand and their catalytic behavior in intermolecular hydroamination reactions

Zirconium and titanium complexes 1 and 2, bearing an amine-bridged bis(phenolato) ligand, have been synthesized and characterized. Although 1 and 2 were inactive in catalyzing intermolecular hydroamination reactions, cationic complexes generated in situ f

Gallium trichloride catalyzed hydroamination of alkynes: Scope, limitation, and mechanistic studies by dft

The successful application of gallium trichloride as a catalyst for the intermolecular hydroamination of alkynes with aromatic amines is reported. The reaction is effective with many aniline derivatives and shows exclusive selectivity for the Markovnikov