40594-87-4

Basic information

• Product Name: N-benzhydrylidene-N'-(4-chlorophenyl)-hydrazine
• Synonyms: N-benzhydrylidene-N'-(4-chlorophenyl)-hydrazine
• CAS NO: 40594-87-4
• Molecular Weight: 306.794
• Mol File: 40594-87-4.mol
• Article Data: 14

Chemical Properties

• CAS DataBase Reference: N-benzhydrylidene-N'-(4-chlorophenyl)-hydrazine(CAS DataBase Reference)
• NIST Chemistry Reference: N-benzhydrylidene-N'-(4-chlorophenyl)-hydrazine(40594-87-4)
• EPA Substance Registry System: N-benzhydrylidene-N'-(4-chlorophenyl)-hydrazine(40594-87-4)

Safety Data

• Hazardous Substances Data: 40594-87-4(Hazardous Substances Data)

Upstream product

• 106-39-8 bromochlorobenzene 
• 5350-57-2 benzophenone hydrazone 
• 119-61-9 benzophenone 
• 574-66-3 Benzophenone oxime 
• 106-47-8 4-chloro-aniline 
• 106-46-7 para-dichlorobenzene 
• 1073-70-7 4-chlorophenylhydrazine hydrochloride 
• 1073-69-4 N-4-chlorophenylhydrazine 

Downstream Products

• 240482-76-2 N-(4-chlorophenyl)-N-benzyl benzophenone hydrazone 
• 909253-27-6 N'-Benzhydrylidene-N-(4-chlorophenyl)-N-methylhydrazine 
• 1044148-73-3 6-chloro-2,3,4,9-tetrahydro-1-phenyl-2-tosyl-1H-pyrido[3,4-b]indole 
• 30081-56-2 1,3,4-triphenylisoquinoline 
• 102173-26-2 6-chloro-N-benzyl-1,2,3,4-tetrahydrocarbazole 
• 36684-65-8 6-chloro-1,2,3,4-tetrahydrocarbazole 
• 18820-82-1 Pyridine hydrobromide 

Relevant articles and documents

Biarylhydrazine compounds and their adducts and applications in the preparation of antitumor drugs

The present invention discloses a biarylhydrazine compound and its application in the preparation of antitumor drugs, the structure of the arylhydrazine compound as shown in formula I, the adduct is a biarylhydrazine compound on the hydrazine group plus benzyloxycarbonyl glycyl prolyl. The anticancer activity of the biarylhydrazine compounds of the present invention is superior to that of the existing positive control drug procarbazine; its Z-GP adduct can significantly reduce in vitro toxicity and in vivo toxicity to normal cells, and can be excised by FΑP-α enzyme specific hydrolysis in vivo (Z-GP) to release hydrolysate products; its Z-GP adduct can significantly inhibit tumor growth in tumor-bearing nude mice and reduce toxicity to non-target organs.

An efficient transition-metal-free synthesis of 1H-indazoles from arylhydrazones with montmorillonite K-10 under O2 atmosphere

An efficient transition-metal-free synthetic method of 1H-indazoles has been developed. The reaction of arylhydrazones in the presence of montmorillonite K-10 in 1,2-dichlorobenzene at 130 °C afforded 1H-indazoles in good yields most likely via a sequenti

Mild method for the synthesis of 1H-indazoles through oxime-phosphonium ion intermediate

The synthesis of 1H-indazoles from o-aminobenzoximes is achieved via N-N bond formation using triphenylphosphine, I2, and imidazole. Selective formation of oxime-phosphonium ion intermediate in the presence of the amino group is the driving for