28571-11-1

Basic information

• Product Name: N-benzyl-N-nitroso-hydroxylamine
• Synonyms: N-benzyl-N-nitroso-hydroxylamine
• CAS NO: 28571-11-1
• Molecular Weight: 152.153
• Mol File: 28571-11-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N-benzyl-N-nitroso-hydroxylamine(CAS DataBase Reference)
• NIST Chemistry Reference: N-benzyl-N-nitroso-hydroxylamine(28571-11-1)
• EPA Substance Registry System: N-benzyl-N-nitroso-hydroxylamine(28571-11-1)

Safety Data

• Hazardous Substances Data: 28571-11-1(Hazardous Substances Data)

Upstream product

• 29601-98-7 N-benzylhydroxylamine hydrochloride 
• 6921-34-2 benzylmagnesium chloride 
• 75-89-8 2,2,2-trifluoroethanol 
• 25370-91-6 N-benzyl-N'-(4-toluenesulfonyloxy)diimide N-oxide 
• 622-30-0 N-benzyl hydroxylalmine 
• 932-90-1 syn-benzaldehyde oxime 
• 3376-26-9 N-Benzylidenebenzylamine N-oxide 

Downstream Products

• 100-52-7 benzaldehyde 
• 62977-82-6 benzyl oxo(phenyl)acetate 
• 120-51-4 benzoic acid benzyl ester 
• 140-11-4 Benzyl acetate 
• 935-05-7 benzyl nitrite 
• 3378-36-7 α,α-azodioxytoluene 
• 932-90-1 Benzaldoxime 
• 25370-91-6 N-benzyl-N'-(4-toluenesulfonyloxy)diimide N-oxide 
• 23135-13-9 N-nitroso-N-benzyl-O-methylhydroxylamine 
• 404852-15-9 (benzyloxy-NNO-azoxy)phenylmethane 
• 23135-14-0 N,O-dibenzyl-N-nitrosohydroxylamine 

Relevant articles and documents

Synthesis and structure of di(NON-azoxy)formals and some related N-alkyl-N'-alkoxydiazene N-oxides

A series of di(NON-azoxy)formals and some related N-alkyl-N'-alkoxydiazene N-oxides were prepared by the reaction of N-nitrosohydroxylamine salts with dihaloalkanes. The dependence of the yield of di(methyl-NON-azoxy)formal on the reaction conditions and the nature of the cation was studied. The structure of di(methyl-NON-azoxy)formal and di(phenyl-NON-azoxy)formal as well as of the copper tert-butylnitrosohydroxylaminate was established by X-ray diffraction analysis.

Reaction of Sydnones with Oxygen

The reaction of 3-benzyl- and 3-(p-chlorobenzyl)-4-phenylsydnones (1a and 1b) and of 3-benzylsydnone (1c) with oxygen at room temperature in the dark is described.Possible rationalizations for the formation of the products obtained are suggested.