3395-76-4

Basic information

• Product Name: Diazene,bis(phenylmethyl)-
• Synonyms: dibenzyl-diazene;[α.α']Azotoluol;azodibenzyl;azotoluene;1,4-diphenylazomethane;ω,ω'-azotoluene
• CAS NO: 3395-76-4
• Molecular Formula: C14H14N2
• Molecular Weight: 210.279
• Mol File: 3395-76-4.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 304.9±31.0 °C(Predicted)
• Density: 0.99±0.1 g/cm3(Predicted)
• CAS DataBase Reference: Diazene,bis(phenylmethyl)- (CAS DataBase Reference)
• NIST Chemistry Reference: Diazene,bis(phenylmethyl)- (3395-76-4)
• EPA Substance Registry System: Diazene,bis(phenylmethyl)- (3395-76-4)

Safety Data

• Hazardous Substances Data: 3395-76-4(Hazardous Substances Data)

Upstream product

• 7626-68-8 N,N'-dibenzylhydrazine 
• 100-46-9 benzylamine 
• 26254-04-6 N,N'-dibenzyl-hydrazine; hydrochloride 
• 7664-41-7 ammonia 
• 7732-18-5 water 
• 7722-84-1 dihydrogen peroxide 
• 7705-08-0 iron(III) chloride 

Downstream Products

• 13211-11-5 benzaldehyde benzylhydrazone 
• 10264-12-7 N-benzylpropanamide 
• 104936-68-7 1-Benzyl-5-ethyl-3-phenyl-1H-[1,2,4]triazole 
• 103-29-7 1,1'-(1,2-ethanediyl)bisbenzene 
• 104936-67-6 1-benzyl-5-methyl-3-phenyl-1H-1,2,4-triazole 
• 588-46-5 N-(phenylmethyl)acetamide 
• 2362-50-7 thianthrene-5-oxide 
• 78075-59-9 4-benzyl-1-naphthalenecarbonitrile 
• 7626-68-8 N,N'-dibenzylhydrazine 
• 2154-56-5 benzyl radical 
• 124116-92-3 1,2-dibenzyl-4,4-diphenyl-[1,2]diazetidin-3-one 
• 588-59-0 stilbene 
• 806-69-9 1,2,3,4-tetraphenylbutane 
• 108-88-3 toluene 

Relevant articles and documents

Improved Process for Preparing Alicyclic Diamine

The present invention relates to a method for synthesizing an alicyclic diamine compound. Provided is a method for producing bicyclohexanediamines in a higher yield while inhibiting production of an aromatic byproduct.COPYRIGHT KIPO 2018

NOVEL OXIDATION OF 1,2-DIBENZYLHYDRAZINES WITH CARBON TETRACHLORIDE

1,2-Dibenzylhydrazines are cleanly oxidized to the corresponding ω,ω'-azotoluenes by carbon tetrachloride; carried out under phase-transfer conditions in the presence of sodium carbonate, the new reaction provides a clean, inexpensive, nearly quantitative route to the azotoluenes.