956-07-0

Basic information

• Product Name: N-Benzoyl-N'-benzylidenehydrazine
• Synonyms: 1-Benzoyl-2-benzylidenehydrazine;Benzaldehyde benzoylhydrazone;N2-Benzylidenebenzoyl hydrazide;N-Benzoyl-N'-benzylidenehydrazine;N'-Benzylidenebenzhydrazide;N'-Benzylidenebenzohydrazide
• CAS NO: 956-07-0
• Molecular Formula: C₁₄H₁₂N₂O
• Molecular Weight: 224.2579
• Mol File: 956-07-0.mol
• Article Data: 71

Chemical Properties

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Appearance: /
• Density: 1.07g/cm³
• CAS DataBase Reference: N-Benzoyl-N'-benzylidenehydrazine(CAS DataBase Reference)
• NIST Chemistry Reference: N-Benzoyl-N'-benzylidenehydrazine(956-07-0)
• EPA Substance Registry System: N-Benzoyl-N'-benzylidenehydrazine(956-07-0)

Safety Data

• Hazardous Substances Data: 956-07-0(Hazardous Substances Data)

Upstream product

• 5281-18-5 benzaldehyde, hydrazone 
• 93-89-0 benzoic acid ethyl ester 
• 13286-78-7 bis-benzoylmercapto-phenyl-methane 
• 60339-73-3 N'-benzylidene-benzohydrazonoyl azide 
• 141-52-6 sodium ethanolate 
• 538-51-2 benzylidene phenylamine 
• 613-94-5 benzoic acid hydrazide 
• 100-52-7 benzaldehyde 
• 622-30-0 N-benzyl hydroxylalmine 
• 19179-24-9 N-Hydroperoxymethyl-N'-benzoylhydrazin 
• 41804-90-4 N-Benzoyl-N-trifylhydrazin 
• 100-39-0 benzyl bromide 
• 110-86-1 pyridine 
• 6830-78-0 3,6-diphenyl-1,2,4,5-tetrazine 

Downstream Products

• 725-12-2 2,5-bis-(phenyl)-1,3,4-oxadiazole 
• 1456-21-9 diphenyl-[1,3,4]thiadiazole 
• 28867-76-7 benzaldehyde benzylidenehydrazone 
• 1215-52-7 N-benzoyl-N'-benzylhydrazine 
• 13864-76-1 3-acetyl-2,3-dihydro-2,5-diphenyl-1,3,4-oxadiazole 
• 1924-86-3 benzaldehyde N-methyl-N-benzoylhydrazone 
• 88246-18-8 C₂₁H₁₈N₂OS₂ 
• 32252-82-7 1-chloro-1,4-diphenyl-2,3-diazabutadiene 
• 100-52-7 benzaldehyde 
• 100-47-0 benzonitrile 
• 92311-69-8 N-(3-Chloro-2-oxo-4-phenyl-azetidin-1-yl)-benzamide 
• 55595-96-5 diethyl <1-(diethoxyphosphinyl)-1-phenylmethyl>phosphoramidate 
• 55-21-0 benzamide 
• 100-46-9 benzylamine 

Relevant articles and documents

Analogs of Nitrofuran Antibiotics to Combat Resistance

-

Analogs of nitrofuran antibiotics are potent GroEL/ES inhibitor pro-drugs

In two previous studies, we identified compound 1 as a moderate GroEL/ES inhibitor with weak to moderate antibacterial activity against Gram-positive and Gram-negative bacteria including Bacillus subtilis, methicillin-resistant Staphylococcus aureus, Kleb

Sodium hypochlorite-mediated synthesis of 2,5-disubstituted 1,3,4-oxadiazoles from hydrazides and aldehydes

[Figure not available: see fulltext.] A simple and convenient method for the synthesis of 2,5-disubstituted 1,3,4-oxadiazoles has been developed. Structurally divergent symmetrical and unsymmetrical 2,5-disubstituted 1,3,4-oxadiazoles can be obtained in moderate to high yields via NaOCl-mediated oxidative cyclization of N-acylhydrazones, generated in situ from aliphatic and aromatic hydrazides and aldehydes.