72867-29-9

Basic information

• Product Name: Benzeneacetonitrile, 3-chloro-a-(phenylamino)-
• CAS NO: 72867-29-9
• Molecular Formula: C14H11ClN2
• Molecular Weight: 242.708
• Mol File: 72867-29-9.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: Benzeneacetonitrile, 3-chloro-a-(phenylamino)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzeneacetonitrile, 3-chloro-a-(phenylamino)-(72867-29-9)
• EPA Substance Registry System: Benzeneacetonitrile, 3-chloro-a-(phenylamino)-(72867-29-9)

Safety Data

• Hazardous Substances Data: 72867-29-9(Hazardous Substances Data)

Upstream product

• 7677-24-9 trimethylsilyl cyanide 
• 587-04-2 m-Chlorobenzaldehyde 
• 98-95-3 nitrobenzene 
• 32347-04-9 N-(3-chlorobenzylidene)aniline 
• 62-53-3 aniline 
• 97070-75-2 2-(3-chlorophenyl)-2-hydroxyacetonitrile 
• 557-21-1 zinc(II) cyanide 

Downstream Products

• 10359-19-0 N-(m-chlorobenzyl)aniline 
• 72867-64-2 N-[1-(3-Chloro-phenyl)-1-cyano-2-phenyl-ethyl]-N-phenyl-benzamide 
• 62482-45-5 1-(m-chlorophenyl)-2-phenylethanone 
• 72867-38-0 N-[(3-Chloro-phenyl)-cyano-methyl]-N-phenyl-benzamide 

Relevant articles and documents

Synthesis and characterization of Pd supported on methane diamine (propyl silane) functionalized Fe3O4 nanoparticles as a magnetic catalyst for synthesis of α-aminonitriles and 2-methoxy-2-phenylacetonitrile derivative via Strecker-t

Pd supported on methane diamine (propyl silane) functionalized Fe3O4 magnetic nanoparticles as an organic–inorganic hybrid heterogeneous catalyst was fabricated and characterized by FT-IR, XRD, SEM, TEM, TGA, VSM, EDX, and ICP-AES te

KF/clinoptilolite nanoparticles as an efficient nanocatalyst for the Strecker synthesis of α-aminonitriles

Abstract: Potassium fluoride impregnated on clinoptilolite nanoparticles (KF/CP NPs) have been explored to serve as an effective and inexpensive heterogeneous catalyst for the one-pot three-component Strecker synthesis of a variety of α-aminonitriles at room temperature in ethanol as a green solvent. KF/CP NPs have been synthesized using simple impregnation techniques in aqueous media from readily available inexpensive starting materials and displayed its initial catalytic activity even after five runs. The easy preparation and separation of catalyst, simple procedure, mild reaction conditions, and excellent yields of products render this method as an attractive sustainable option. Graphic abstract: [Figure not available: see fulltext.]

Three-component solventless Strecker synthesis of α-aminonitriles catalysed by a renewable sulfonated nanoporous carbon catalyst (CMK-5-SO3H)

The one-pot three-component synthesis of a variety of α-aminonitriles has been studied using a catalytic amount of a sulfonic acid-functionalized ordered nanoporous carbon catalyst, CMK-5-SO3H, at room temperature under solvent-free reaction co