176036-82-1

Basic information

• Product Name: N-(3,5-dichlorophenyl)benzamide (3,5-dichlorophenyl)hydrazone
• Synonyms: N-(3,5-dichlorophenyl)benzamide (3,5-dichlorophenyl)hydrazone
• CAS NO: 176036-82-1
• Molecular Weight: 425.144
• Mol File: 176036-82-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-(3,5-dichlorophenyl)benzamide (3,5-dichlorophenyl)hydrazone(CAS DataBase Reference)
• NIST Chemistry Reference: N-(3,5-dichlorophenyl)benzamide (3,5-dichlorophenyl)hydrazone(176036-82-1)
• EPA Substance Registry System: N-(3,5-dichlorophenyl)benzamide (3,5-dichlorophenyl)hydrazone(176036-82-1)

Safety Data

• Hazardous Substances Data: 176036-82-1(Hazardous Substances Data)

Upstream product

• 15999-94-7 N-(3,5-dichlorophenyl)benzimidoyl chloride 
• 39943-56-1 3,5-dichlorophenylhydrazine 

Relevant articles and documents

7. The chemistry of stable carbenes: Part 2 - Benzoin-type condensations of formaldehyde catalyzed by stable carbenes

Stable carbenes derived from thiazole, 1 H-imidazole, and 4H -1,2,4-triazole are efficient catalysts for benzoin-type condensations of formaldehyde. Catalysts derived from N-substituted thiazolium salts trimerize formaldehyde to dihydroxyacetone (II). Catalysts based on 1,4-disubstituted 4H-1,2,4-triazol-1-ium salts give glycolaldehyde (I) as the main product and no II, whereas N,N′-disubstituted 1H-imidazol-3-ium salts yield mixtures of both products. The isolation of several intermediates in the catalytic cycle provide a better insight into the reaction mechanism.