65783-00-8

Basic information

• Product Name: Benzeneacetonitrile, a-methyl-2-nitro-
• CAS NO: 65783-00-8
• Molecular Formula: C9H8N2O2
• Molecular Weight: 176.175
• Mol File: 65783-00-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzeneacetonitrile, a-methyl-2-nitro-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzeneacetonitrile, a-methyl-2-nitro-(65783-00-8)
• EPA Substance Registry System: Benzeneacetonitrile, a-methyl-2-nitro-(65783-00-8)

Safety Data

• Hazardous Substances Data: 65783-00-8(Hazardous Substances Data)

Upstream product

• 610-66-2 2-nitro-benzeneacetonitrile 
• 69642-00-8 α-methyl-o-nitrobenzyl bromide 
• 65548-02-9 (+/-)-ethyl cyano(2-nitrophenyl)acetate 
• 88975-16-0 Cyano-methyl-(2-nitro-phenyl)-acetic acid ethyl ester 
• 88-73-3 2-Chloronitrobenzene 

Downstream Products

• 88975-17-1 2-(2-aminophenyl)propionitrile 
• 56355-31-8 2-[4-(methyl-thiazol-2-yl-amino)-phenyl]-propionic acid 
• 88975-44-4 2-(2-Hydroxy-phenyl)-propionitrile 
• 88975-27-3 2-(2-methylaminophenyl)propionitrile 
• 88975-94-4 2-(2-Cyanato-phenyl)-propionitrile 
• 88976-04-9 N-[2-(Cyano-methyl-methyl)-phenyl]-2,2,2-trifluoro-acetamide 
• 88975-49-9 2-<2-(2-thiazolylamino)phenyl>propionic acid 
• 88975-97-7 2-<2-(2-thiazolyloxy)phenyl>propionic acid 
• 88975-79-5 2-<2-(N-methyl-N-thiazol-2-ylamino)phenyl>propionic acid 
• 88975-59-1 1-Benzoyl-3-[2-(cyano-methyl-methyl)-phenyl]-thiourea 
• 88975-74-0 3-Benzoyl-1-[2-(cyano-methyl-methyl)-phenyl]-1-methyl-thiourea 
• 25798-61-2 ortho-nitroso acetophenone 
• 83-34-1 3-Methylindole 

Relevant articles and documents

Active and Recyclable Catalytic Synthesis of Indoles by Reductive Cyclization of 2-(2-Nitroaryl)acetonitriles in the Presence of Co-Rh Heterobimetallic Nanoparticles with Atmospheric Hydrogen under Mild Conditions

A cobalt-rhodium heterobimetallic nanoparticle-catalyzed reductive cyclization of 2-(2-nitroaryl)acetonitriles to indoles has been achieved. The tandem reaction proceeds without any additives under the mild conditions (1 atm H2 and 25 °C). This procedure could be scaled up to the gram scale. The catalytic system is significantly stable under these reaction conditions and could be reused more than ten times without loss of catalytic activity.

A caged cyanide

A photoactivatable caged cyanide, 1-(2-nitrophenyl)ethyl (NPE) cyanide, was synthesized, which upon irradiation in the near UV releases cyanide. It is demonstrated that the compound can be used to induce formation of the Fe III-CN- complex in the heme protein nitrophorin 4 from Rhodnius prolixus.