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CAS 337508-64-2

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5-phenyl-1,3-oxazole-4-carbonyl chloride

Description:
5-Phenyl-1,3-oxazole-4-carbonyl chloride is a chemical compound characterized by its oxazole ring structure, which features a phenyl group and a carbonyl chloride functional group. This compound typically exhibits properties associated with both aromatic and heterocyclic compounds, including stability and reactivity due to the presence of the carbonyl chloride, which is a reactive electrophile. The oxazole ring contributes to its potential as a building block in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. The presence of the phenyl group enhances its lipophilicity, which can influence its biological activity and solubility in organic solvents. Additionally, the carbonyl chloride functionality allows for further derivatization, making it a versatile intermediate in chemical reactions. Safety considerations should be taken into account due to the reactivity of the carbonyl chloride, which can release hydrochloric acid upon hydrolysis. Overall, this compound is of interest in synthetic organic chemistry for its potential applications in various fields.
Formula:C10H6ClNO2
InChI:InChI=1/C10H6ClNO2/c11-10(13)8-9(14-6-12-8)7-4-2-1-3-5-7/h1-6H
SMILES:c1ccc(cc1)c1c(C(=O)Cl)nco1
Synonyms:
  • 5-Phenyloxazole-4-Carbonyl Chloride
  • 4-(Chlorocarbonyl)-5-phenyl-1,3-oxazole
  • 4-Oxazolecarbonyl chloride, 5-phenyl-
  • 5-Phenyl-1,3-oxazole-4-carbonyl chloride ,97%
  • 4-Oxazolecarbonyl chloride, 5-phenyl- (9CI)
  • 5-PHENYL-1,3-OXAZOLE-4-CARBONYL CHLORIDE
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