49615-69-2

Basic information

• Product Name: 4-(4-METHOXYPHENYL)-1,2,5-OXADIAZOL-3-AMINE
• Synonyms: 4-(4-METHOXYPHENYL)-1,2,5-OXADIAZOL-3-AMINE;AKOS BBS-00005836
• CAS NO: 49615-69-2
• Molecular Formula: C₉H₉N₃O₂
• Molecular Weight: 191.19
• Mol File: 49615-69-2.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-(4-METHOXYPHENYL)-1,2,5-OXADIAZOL-3-AMINE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(4-METHOXYPHENYL)-1,2,5-OXADIAZOL-3-AMINE(49615-69-2)
• EPA Substance Registry System: 4-(4-METHOXYPHENYL)-1,2,5-OXADIAZOL-3-AMINE(49615-69-2)

Safety Data

• Hazard Codes: Xn
• Statements: 22
• Hazardous Substances Data: 49615-69-2(Hazardous Substances Data)

Upstream product

• 38435-51-7 N-hydroxy-4-methoxy-benzenecarboximidoyl chloride 
• 3717-21-3 p-methoxyl benzaldoxime 
• 1823-76-3 p-methoxy-isonitrosoacetophenone 
• 22027-50-5 methyl 3-(4-methoxybenzoyl)acetate 
• 14271-83-1 4-methoxybenzoyl cyanide 

Downstream Products

• 49615-80-7 2-acetyl-3-[4-(4-methoxy-phenyl)-furazan-3-ylamino]-acrylic acid ethyl ester 
• 49615-79-4 {[4-(4-methoxy-phenyl)-furazan-3-ylamino]-methylene}-malonic acid diethyl ester 
• 49615-81-8 2-cyano-3-[4-(4-methoxy-phenyl)-furazan-3-ylamino]-acrylic acid ethyl ester 
• 49615-74-9 N'-[4-(4-methoxy-phenyl)-furazan-3-yl]-N,N-dimethyl-formamidine 
• 49615-73-8 benzylidene-[4-(4-methoxy-phenyl)-furazan-3-yl]-amine 

Relevant articles and documents

N -Oxide-Controlled Chemoselective Reduction of Nitrofuroxans

A facile and chemoselective SnCl 2 -mediated mild reduction of regioisomeric 3- and 4-nitrofuroxans for the synthesis of aminofurazans and aminofuroxans in good yields is developed. Reduction of 4-nitrofuroxans results in the selective formation of 4-aminofuroxans, while analogous reduction of 3-nitrofuroxans affords 3-aminofurazans as a result of simultaneous reduction of the nitro group and exocyclic N-O bond.

One-pot synthesis of 3-amino-4-aryl- and 3-amino-4-hetarylfurazans

A "one pot" method for the synthesis of 3-amino-4-aryl- and 3-amino-4-hetarylfurazans from β-aryl- and 4-β-hetaryl-β-oxo acid esters was developed.