CAS 3356-96-5

ethyl 5-chloro-4-methyl-1,2-oxazole-3-carboxylate

Description:

Ethyl 5-chloro-4-methyl-1,2-oxazole-3-carboxylate is a chemical compound characterized by its oxazole ring, which is a five-membered heterocyclic structure containing both nitrogen and oxygen. This compound features a chloro substituent at the 5-position and a methyl group at the 4-position of the oxazole ring, contributing to its unique reactivity and properties. The presence of the ethyl ester group at the 3-position enhances its solubility in organic solvents and may influence its biological activity. Ethyl 5-chloro-4-methyl-1,2-oxazole-3-carboxylate is typically used in organic synthesis and may serve as an intermediate in the preparation of various pharmaceuticals or agrochemicals. Its molecular structure suggests potential applications in medicinal chemistry, particularly due to the presence of the oxazole moiety, which is known for its diverse biological activities. As with many chemical substances, safety precautions should be observed when handling this compound, including the use of appropriate personal protective equipment and adherence to safety data sheet guidelines.

Formula: C₇H₈ClNO₃

InChI: InChI=1/C7H8ClNO3/c1-3-11-7(10)5-4(2)6(8)12-9-5/h3H2,1-2H3

SMILES: CCOC(=O)c1c(C)c(Cl)on1

Synonyms:

• 3-Isoxazolecarboxylic Acid, 5-Chloro-4-Methyl-, Ethyl Ester
• Ethyl 5-chloro-4-methyl-1,2-oxazole-3-carboxylateethyl 5-chloro-4-methylisoxazole-3-carboxylate
• Ethyl 5-chloro-4-methylisoxazole-3-carboxylate
• ethyl 5-chloro-4-Methyl-1,2-oxazole-3-carboxylate
• 5-chloro-4-Methylisoxazole-3-carboxylate

Ethyl 5-chloro-4-methylisoxazole-3-carboxylate

CAS: 3356-96-5

Ethyl 5-chloro-4-methylisoxazole-3-carboxylate

Purity: 95%

Molecular weight: 189.60g/mol

Ref: 54-OR904439