57767-04-1

Basic information

• Product Name: p-nitro-N-phenylbenzamide oxime
• Synonyms: p-nitro-N-phenylbenzamide oxime
• CAS NO: 57767-04-1
• Molecular Weight: 257.249
• Mol File: 57767-04-1.mol

Chemical Properties

• CAS DataBase Reference: p-nitro-N-phenylbenzamide oxime(CAS DataBase Reference)
• NIST Chemistry Reference: p-nitro-N-phenylbenzamide oxime(57767-04-1)
• EPA Substance Registry System: p-nitro-N-phenylbenzamide oxime(57767-04-1)

Safety Data

• Hazardous Substances Data: 57767-04-1(Hazardous Substances Data)

Upstream product

• 62-53-3 aniline 
• 1011-84-3 4-nitrobenzohydroximoyl chloride 
• 555-16-8 4-nitrobenzaldehdye 
• 1129-37-9 4-nitrobenzaldehyde oxime 

Downstream Products

• 139488-19-0 4-nitrobenzanilide oxime phenylcarbamate 
• 1932-32-7 N-(4-nitrophenyl)-N'-phenylurea 
• 729-13-5 2-(4-nitrophenyl)benzimidazole 
• 619-72-7 4-nitrobenzonitrile 
• 22347-65-5 4-(4-nitro-phenyl)-3-phenyl-2-phenylimino-2,3-dihydro-2λ⁴-[1,2,3,5]oxathiadiazole 
• 60404-72-0 (4-nitro-phenyl)-[3-(4-nitro-phenyl)-4-phenyl-4H-[1,2,4]oxadiazol-5-ylidene]-amine 
• 22347-62-2 2-benzenesulfonylimino-4-(4-nitro-phenyl)-3-phenyl-2,3-dihydro-2λ⁴-[1,2,3,5]oxathiadiazole 
• 24794-13-6 1-[3-(4-nitro-phenyl)-4-phenyl-4H-[1,2,4]oxadiazol-5-ylidene]-propan-2-one 

Relevant articles and documents

Practical synthesis of N -substituted cyanamides via tiemann rearrangement of amidoximes

A facile and general synthesis of various N-substituted cyanamides was accomplished by the Tiemann rearrangement of amidoximes with benzenesulfonyl chlorides (TsCl or o-NsCl) and DIPEA.

REACTIONS OF ORTHOFORMIC ESTER WITH MONOSUBSTITUTED AMIDE OXIMES

In the reactions of N-monosubstituted p-nitrobenzamide oximes with orthoformic ester in presence of boron trifluoride ether complex p-nitrobenzonitrile and a carbamate of the original amide oxime are formed.Under the same condition bis(methylamino)glyoxime gives a 1-cyano-N-methylformamide oxime carbamate.