579-45-3

Basic information

• Product Name: N-phenylbenzohydrazide
• Synonyms: Benzoic acid, phenylhydrazide
• CAS NO: 579-45-3
• Molecular Formula: C₁₃H₁₂N₂O
• Molecular Weight: 212.2472
• Mol File: 579-45-3.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 358.7°C at 760 mmHg
• Flash Point: 170.7°C
• Density: 1.219g/cm³
• Vapor Pressure: 2.5E-05mmHg at 25°C
• Refractive Index: 1.662
• CAS DataBase Reference: N-phenylbenzohydrazide(CAS DataBase Reference)
• NIST Chemistry Reference: N-phenylbenzohydrazide(579-45-3)
• EPA Substance Registry System: N-phenylbenzohydrazide(579-45-3)

Safety Data

• Hazardous Substances Data: 579-45-3(Hazardous Substances Data)

Upstream product

• 64-19-7 acetic acid 
• 7647-01-0 hydrogenchloride 
• 7664-93-9 sulfuric acid 
• 100-63-0 phenylhydrazine 
• 98-88-4 benzoyl chloride 
• 42116-43-8 tert-butyl 2-phenylhydrazine-1-carboxylate 
• 114-83-0 1-acetyl-2-phenylhydrazine 
• 60295-43-4 N-benzoyl-N-phenyl-N'-tert-butoxycarbonyl hydrazine 
• 71-43-2 benzene 
• 59105-56-5 phenyl-hydrazine; sodium-compound 
• 5014-47-1 N-chloro-N-phenylbenzamide 
• 70609-11-9 N-Benzoyl-N'-acetyl-phenylhydrazine 

Downstream Products

• 70609-11-9 N-Benzoyl-N'-acetyl-phenylhydrazine 
• 21005-31-2 benzoic acid-(benzylidene-phenyl-hydrazide) 
• 5455-22-1 1,2-dibenzoyl-1-phenylhydrazine 
• 116557-69-8 benzoic acid-(5-methyl-2-phenylazo-phenyl ester) 
• 19374-75-5 3-methyl-1-phenylpyrazole-4,5-dione 4-phenylhydrazone 
• 76033-80-2 1-benzoyl-1-phenyl semicarbazide 
• 93-98-1 N-phenyl benzoyl amide 
• 614-31-3 N-benzyl-N-phenylhydrazine 
• 99801-56-6 3,6-anhydro-L-galactose-(benzyl-phenyl-hydrazone) 

Relevant articles and documents

Four Simultaneously Dynamic Covalent Reactions. Experimental Proof of Orthogonality

Dynamic covalent reactions are widely used in dynamic combinatorial chemistry. Most of these reactions are run under differing reaction conditions and exhibit cross-reactivity when components of multiple reactions are present in one reaction vessel. Herei

Photoinduced cleavage of N-N bonds of aromatic hydrazines and hydrazides by visible light

A photocatalytic system involving [Ru(bpyrz)(PFH, visible light, and air has been developed for cleavage of the N-N bonds of hydrazines and hydrazides. This catalytic system is generally effective for N,N-disubstituted hydrazine and hydrazide derivatives, including arylhydrazides, N-alkyl-N-arylhydrazines, and N,N-diarylhydrazines. The utility of this cleavage reaction has been demonstrated by synthesizing a variety of secondary aromatic amines. Georg Thieme Verlag Stuttgart ? New York.