17359-83-0

Basic information

• Product Name: N'-(2,4-dinitrophenyl)benzhydrazide
• Synonyms: N'-(2,4-dinitrophenyl)benzhydrazide
• CAS NO: 17359-83-0
• Molecular Weight: 320.692
• Mol File: 17359-83-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N'-(2,4-dinitrophenyl)benzhydrazide(CAS DataBase Reference)
• NIST Chemistry Reference: N'-(2,4-dinitrophenyl)benzhydrazide(17359-83-0)
• EPA Substance Registry System: N'-(2,4-dinitrophenyl)benzhydrazide(17359-83-0)

Safety Data

• Hazardous Substances Data: 17359-83-0(Hazardous Substances Data)

Upstream product

• 98-88-4 benzoyl chloride 
• 119-26-6 (2,4-dinitro-phenyl)-hydrazine 
• 93-97-0 benzoic acid anhydride 
• 39209-17-1 N'-(2,4-dinitrophenyl)benzhydrazide 
• 1157-84-2 1-benzylidene-2-(2,4-dinitrophenyl)hydrazone 

Downstream Products

• 155951-51-2 7-Amino-2-phenyl-5H-[1,2,4]triazolo[1,5-a]quinoxalin-4-one 
• 155951-47-6 ethyl 1-(2,4-dinitrophenyl)-3-phenyl-1,2,4-triazole-5-carboxylate 
• 155951-44-3 N¹-(2,4-Dinitrophenyl)-N³-ethoxalyl-N²-benzamidrazone 
• 115591-33-8 C₁₃H₁₁N₅O₄ 

Relevant articles and documents

An approach to pyrazoline-fused chlorins by dipolar [3 + 2]-cycloaddition of iminonitriles to Meso-Tetrakis(pentafluorophenyl)porphyrin: Synthesis of new PDT photosensitizers

Meso-Tetrakis(pentafluorophenyl)porphyrin reacts at higher temperature with unstable iminonitriles (RC≡N+-N--Ar), affording pyrazoline-fused chlorins, according to dipolar [3 + 2]-cycloaddition pathway. The respective iminonitriles were in situ generated from the corresponding functionalized α-halogenohydrazine derivatives by 1,3-elimination of HX in the presence of base (NEt3, DABCO). This method allows synthesis of very attractive moieties which may be of potential use as sensitizers in photodynamic therapy (PDT).

Halogenation of Substituted Hydrazones. A Facile Route for the Synthesis of Some New Hydrazidoyl Halides

A wide variety of new alkyl, aryl, acyl and ethoxycarbonyl derivatives of hydrazidoyl halides have been synthesized by the electrophilic attack of the halogen atom on the corresponding hydrazone chain.The structural assignments of the products are based o