1443438-81-0

Basic information

• Product Name: 3-{5-[(E)-2-(4-chlorophenyl)-1-ethenyl]-1,3,4-oxadiazol-2-yl}-3-hydroxy-2-butanone
• Synonyms: 3-{5-[(E)-2-(4-chlorophenyl)-1-ethenyl]-1,3,4-oxadiazol-2-yl}-3-hydroxy-2-butanone
• CAS NO: 1443438-81-0
• Molecular Weight: 292.722
• Mol File: 1443438-81-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3-{5-[(E)-2-(4-chlorophenyl)-1-ethenyl]-1,3,4-oxadiazol-2-yl}-3-hydroxy-2-butanone(CAS DataBase Reference)
• NIST Chemistry Reference: 3-{5-[(E)-2-(4-chlorophenyl)-1-ethenyl]-1,3,4-oxadiazol-2-yl}-3-hydroxy-2-butanone(1443438-81-0)
• EPA Substance Registry System: 3-{5-[(E)-2-(4-chlorophenyl)-1-ethenyl]-1,3,4-oxadiazol-2-yl}-3-hydroxy-2-butanone(1443438-81-0)

Safety Data

• Hazardous Substances Data: 1443438-81-0(Hazardous Substances Data)

Upstream product

• 1615-02-7 3-(4-chlorophenyl)prop-2-enoic acid 
• 73789-56-7 N-isocyaniminotriphenylphosphorane 
• 431-03-8 dimethylglyoxal 

Relevant articles and documents

Three-component reaction of N-isocyaniminotriphenylphosphorane (Ph 3PNNC), biacetyl, and a carboxylic acid in water

Reaction of N-isocyaniminotriphenylphosphorane with biacetyl in the presence of a carboxylic acid in water proceeds smoothly at RT (20-26°C) and neutral conditions to afford sterically congested 1,3,4-oxadiazole derivatives in high yields. The reaction pr

The reaction of N -isocyaniminotriphenylphosphorane with biacetyl in the presence of (E) -cinnamic acids: Synthesis of fully substituted 1,3,4-oxadiazole derivatives via intramolecular aza -wittig reactions of in situ generated iminophosphoranes

Reaction of N-isocyaniminotriphenylphosphorane with biacetyl in the presence of (E)-cinnamic acids proceeds smoothly at room temperature and under neutral conditions to afford sterically congested 1,3,4-oxadiazole derivatives in high yields. The reaction