71297-93-3

Basic information

• Product Name: (Z)-1,2-bis(4-chlorophenyl)diazene 1-oxide
• CAS NO: 71297-93-3
• Molecular Weight: 267.114
• Mol File: 71297-93-3.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: (Z)-1,2-bis(4-chlorophenyl)diazene 1-oxide(CAS DataBase Reference)
• NIST Chemistry Reference: (Z)-1,2-bis(4-chlorophenyl)diazene 1-oxide(71297-93-3)
• EPA Substance Registry System: (Z)-1,2-bis(4-chlorophenyl)diazene 1-oxide(71297-93-3)

Safety Data

• Hazardous Substances Data: 71297-93-3(Hazardous Substances Data)

Upstream product

• 100-00-5 4-chlorobenzonitrile 
• 128479-43-6 N-isobutyl-N-(4-chlorophenyl)amine 
• 106-47-8 4-chloro-aniline 
• 68-12-2 N,N-dimethyl-formamide 
• 1602-00-2 bis-(4-chloro-phenyl)-diazene 

Downstream Products

• 21650-51-1 (E)-bis(4-chlorophenyl)diazene 
• 1421276-55-2 2-(4-chlorophenyl)-3-phenyl-5-chloro-2H-indazole 

Relevant articles and documents

A Highly Selective Amidation of Azoxybenzenes with Sulfonamides via Rhodium(III)-Catalyzed C-H Activation

A new amidation of azoxybenzenes with sulfonamides catalyzed by a rhodium(III) salt has been developed. This sulfonamidation proceeds efficiently under mild reaction conditions to generate new C-N bonds through C-H bond activation and functionalization, affording the corresponding 2-sulfonamidoazoxybenzenes in good yields with high regioselectivity.

Convergent Paired Electrochemical Synthesis of Azoxy and Azo Compounds: An Insight into the Reaction Mechanism

A convergent paired electrochemical method was developed for the synthesis of azoxy and azo compounds starting from the corresponding nitroarenes. We propose a unique mechanism for electrosynthesis of azoxy and azo compounds. We find that both anodic and cathodic reactions are responsible for the synthesis of these compounds. The synthesis of azoxy and azo derivatives have been successfully performed in an undivided cell, using carbon rod electrodes, by constant current electrolysis at room temperature.

Catalytic Selective Oxidative Coupling of Secondary N-Alkylanilines: An Approach to Azoxyarene

Azoxyarenes are among important scaffolds in organic molecules. Direct oxidative coupling of primary anilines provides a concise fashion to construct them. However, whether these scaffolds can be prepared from secondary N-alkylanilines is not well explored. Here, we present a catalytic selective oxidative coupling of secondary N-alkylaniline to afford azoxyarene with tungsten catalyst under mild conditions. In addition, azoxy can be viewed as a bioisostere of alkene and amide. Several "azoxyarene analogues" of the corresponding bioactive alkenes and amides showed comparable promising anticancer activities.