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1,2,3-Oxadiazole

Base Information
  • Chemical Name:1,2,3-Oxadiazole
  • CAS No.:288-43-7
  • Molecular Formula:C2H2N2O
  • Molecular Weight:70.0507
  • Hs Code.:2934999090
  • Mol file:288-43-7.mol
1,2,3-Oxadiazole

Synonyms:[1,2,3]oxadiazole;polyoxadiazole;oxdiazole;oxadiazole acid;oxadiazole radical;oxadiazole;

Suppliers and Price of 1,2,3-Oxadiazole
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
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  • Chemicals and raw materials
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Total 4 raw suppliers
Chemical Property of 1,2,3-Oxadiazole
Chemical Property:
  • PSA:38.92000 
  • LogP:0.06960 
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Description 1,2,3-Oxadiazole is a five-membered, unsaturated, unstable, nonbenzenoid, heteroaromatic, comprised of two carbon atoms, one oxygen atom, and two pyridine-type nitrogen atoms linked in continuity (O-N-N). Depending on the position of the nitrogen atoms, the four possible regioisomeric structures are generated for oxadiazoles. The cyclic structure for 1,2,3-oxadiazoles is unstable and readily isomerizes to α-diazoketone, an open chain structure.
  • Physical properties 3-Phenylsydnone is a crystalline compound prone to hydrolysis with ring cleavage, especially in basic medium. The carbonyl stretching frequency in the IR spectra of sydnones is found in the range of 1720–1790 cm–1 depending on the substituent present. The UV spectra of alkylsydnones showed a single maxima at 290 nm.
Technology Process of 1,2,3-Oxadiazole

There total 16 articles about 1,2,3-Oxadiazole which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 100.0%

Guidance literature:
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