151733-56-1

Basic information

• Product Name: 1,2,5-Oxadiazole-3-carboxaldehyde, 4-phenyl-, oxime, 2-oxide
• CAS NO: 151733-56-1
• Molecular Formula: C9H7N3O3
• Molecular Weight: 205.173
• Mol File: 151733-56-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1,2,5-Oxadiazole-3-carboxaldehyde, 4-phenyl-, oxime, 2-oxide(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2,5-Oxadiazole-3-carboxaldehyde, 4-phenyl-, oxime, 2-oxide(151733-56-1)
• EPA Substance Registry System: 1,2,5-Oxadiazole-3-carboxaldehyde, 4-phenyl-, oxime, 2-oxide(151733-56-1)

Safety Data

• Hazardous Substances Data: 151733-56-1(Hazardous Substances Data)

Upstream product

• 135733-30-1 3-(hydroxymethyl)-4-phenylfuroxan 
• 169614-78-2 3-(bromomethyl)-2-oxido-4-phenyl-1,2,5-oxadiazole 
• 6898-86-8 3-methyl-4-phenylfuroxan 
• 135733-34-5 4-phenylfuroxan-3-carboxaldehyde 

Downstream Products

• 125520-62-9 4-phenyl-3-furoxancarbonitrile 

Relevant articles and documents

Synthesis of furoxan derivatives: DABCO-mediated cascade sulfonylation/cyclization reaction of α-nitro-ketoximes

A convenient and efficient method for the synthesis of furoxan derivatives from α-nitro-ketoximes and sulfonyl chlorides is reported. A wide variety of furoxan derivatives were smoothly obtained in good yields via a DABCO-mediated cascade sulfonylation/cy

Unsymmetrically Substituted Furoxans, XIV. Synthesis and Structure of a Trimer of the Furoxan System with High Vasodilator and Platelet Antiaggregatory Activity

The synthesis and structure of a trimer 5 of the furoxan system are reported.The probable origin of this derivative is the dimerization of the intermediate 4-phenyl-3-furoxancarbonitrile oxide (4) obtained by decomposition of the corresponding nitrolic ac