1330573-06-2

Basic information

• Product Name: 3-nitramino-4-phenyl-1,2,5-oxadiazole
• Synonyms: 3-nitramino-4-phenyl-1,2,5-oxadiazole
• CAS NO: 1330573-06-2
• Molecular Weight: 206.161
• Mol File: 1330573-06-2.mol

Chemical Properties

• CAS DataBase Reference: 3-nitramino-4-phenyl-1,2,5-oxadiazole(CAS DataBase Reference)
• NIST Chemistry Reference: 3-nitramino-4-phenyl-1,2,5-oxadiazole(1330573-06-2)
• EPA Substance Registry System: 3-nitramino-4-phenyl-1,2,5-oxadiazole(1330573-06-2)

Safety Data

• Hazardous Substances Data: 1330573-06-2(Hazardous Substances Data)

Upstream product

• 10349-14-1 4-phenyl-furazan-3-ylamine 

Downstream Products

• 1341124-32-0 3-[methyl(nitro)amino]-4-phenyl-1,2,5-oxadiazole 
• 1341124-31-9 E-3-[methoxy(oxido)diazenyl]-4-phenyl-1,2,5-oxadiazole 
• 10349-14-1 4-phenyl-furazan-3-ylamine 
• 1035831-41-4 3-amino-4-(3'-nitrophenyl)-1,2,5-oxadiazole 
• 114854-42-1 3-amino-4-(4'-nitrophenyl)-1,2,5-oxadiazole 
• 21742-07-4 3-amino-4-(2'-nitrophenyl)-1,2,5-oxadiazole 
• 1341124-34-2 [1,2,5]oxadiazolo[3,4-c]cinnoline 5-N-oxide 

Relevant articles and documents

Nitration of primary aminofurazans with aqueous nitric acid

A convenient procedure for the synthesis of N-nitroaminofurazans by nitration of primary 3-amino-4-R-furazans (R = Me, NO2, phenyl-, methyl-NNO-azoxy-, tert-butyl-NNO-azoxy-, tert-butyldiazenyl-, etc.) with 66-77% aqueous nitric acid was develo

Generation of oxodiazonium ions 1. Synthesis of [1,2,5]oxadiazolo[3,4-c] cinnoline 5-oxides

Methods for the synthesis of [1,2,5]oxadiazolo[3,4-c]cinnoline 5-oxides, which include the reaction of 3-nitramino-4-(R-phenyl)furazans or their O-methyl derivatives with electrophilic agents, have been developed. Unsubstituted [1,2,5]oxadiazolo[3,4-c]cin