34414-10-3

Basic information

• Product Name: Cyanamide, (diphenylmethylene)-
• CAS NO: 34414-10-3
• Molecular Formula: C14H10N2
• Molecular Weight: 206.247
• Mol File: 34414-10-3.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Cyanamide, (diphenylmethylene)-(CAS DataBase Reference)
• NIST Chemistry Reference: Cyanamide, (diphenylmethylene)-(34414-10-3)
• EPA Substance Registry System: Cyanamide, (diphenylmethylene)-(34414-10-3)

Safety Data

• Hazardous Substances Data: 34414-10-3(Hazardous Substances Data)

Upstream product

• 90495-20-8 1-tert-butyl-3-(diphenylmethyl)carbodiimide 
• 7677-24-9 trimethylsilyl cyanide 
• 574-66-3 Benzophenone oxime 
• 1013-88-3 Benzophenone imine 
• 75-05-8 acetonitrile 
• 78-67-1 2,2'-azobis(isobutyronitrile) 
• 25347-82-4 1-tert-butyl-3-(diphenylmethyl)thiourea 
• 78646-42-1 9,10-dihydro-9,10-(N-cyanoepoxyimino)-9,10-dimethylanthracene 
• 908093-98-1 diazodiphenylmethane 
• 4343-68-4 nitrosyl cyanide 
• 75-18-3 dimethylsulfide 
• 119-61-9 benzophenone 
• 1000-70-0 bis(trimethylsilyl)carbodi-imide 

Downstream Products

• 119-61-9 benzophenone 

Relevant articles and documents

Access to Cyanoimines Enabled by Dual Photoredox/Copper-Catalyzed Cyanation of O-Acyl Oximes

An efficient strategy for the synthesis of pharmaceutically important and synthetically useful cyanoimines, as well as cyanamides, has been described. This strategy is enabled by dual photoredox/copper-catalyzed cyanation of O-acyl oximes or O-acyl hydroxamides. This state of the art protocol for cyanoimines and cyanamides features readily available starting materials, mild reaction conditions, good functional group tolerance, and operational simplicity. The resultant cyanoimines can be transformed into structurally diverse and functionally important N-containing heterocycles.

Copper-catalyzed N-cyanation of sulfoximines by AIBN

The direct copper-catalyzed N-cyanation of sulfoximines was achieved by using AIBN as a safe cyanide source. It represents a simple and environmentally benign procedure for the construction of the N-CN bond. Furthermore, some sec-amines can also be tolera

Einstufiger Weg zu N-Cyaniminen und zu N,N'-Dicyanchinondiiminen, einer neuen Klasse von Elektronenacceptoren

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