CAS 64640-13-7
:2-(chloromethyl)-5-phenyl-1,3-oxazole
Description:
2-(Chloromethyl)-5-phenyl-1,3-oxazole is an organic compound characterized by its oxazole ring, which is a five-membered heterocyclic structure containing both nitrogen and oxygen. This compound features a chloromethyl group (-CH2Cl) at the 2-position and a phenyl group (-C6H5) at the 5-position of the oxazole ring, contributing to its reactivity and potential applications in organic synthesis. The presence of the chloromethyl group makes it a useful intermediate in various chemical reactions, including nucleophilic substitution and coupling reactions. The phenyl group enhances the compound's stability and can influence its solubility and interaction with other molecules. Typically, compounds like this may exhibit biological activity, making them of interest in medicinal chemistry. Its CAS number, 64640-13-7, allows for easy identification and retrieval of information in chemical databases. Overall, 2-(chloromethyl)-5-phenyl-1,3-oxazole is a versatile compound with potential applications in pharmaceuticals and materials science.
Formula:C10H8ClNO
InChI:InChI=1/C10H8ClNO/c11-6-10-12-7-9(13-10)8-4-2-1-3-5-8/h1-5,7H,6H2
SMILES:c1ccc(cc1)c1cnc(CCl)o1
Synonyms:- Oxazole, 2-(Chloromethyl)-5-Phenyl-
- 2-(Chloromethyl)-5-phenyl-1,3-oxazole
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Found 2 products.
2-(chloromethyl)-5-phenyl-1,3-oxazole
CAS:<p>2-(Chloromethyl)-5-phenyl-1,3-oxazole is an inhibitor of cholesterol ester transfer protein (CETP) that belongs to the family of amides. It binds to the active site of CETP, preventing it from cleaving cholesteryl esters from HDL and transferring them to LDL. This prevents the formation of cholesteryl ester/LDL complexes, which are believed to be one cause of atherosclerosis. 2-(Chloromethyl)-5-phenyl-1,3-oxazole also inhibits cholesterol synthesis in liver cells by inhibiting HMG CoA reductase.</p>Formula:C10H8ClNOPurity:Min. 95%Molecular weight:193.63 g/mol
