Ethyl 2-(chloromethyl)-1,3-oxazole-4-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 carboxylate group, which contributes to its acidity and reactivity, and a chloromethyl substituent that enhances its electrophilic properties, making it useful in various chemical reactions. Ethyl 2-(chloromethyl)-1,3-oxazole-4-carboxylate is typically a colorless to pale yellow liquid or solid, depending on its purity and specific conditions. It is soluble in organic solvents, which facilitates its use in organic synthesis. The presence of the chloromethyl group allows for further functionalization, making it a valuable intermediate in the synthesis of pharmaceuticals and agrochemicals. Safety data indicates that it should be handled with care, as it may pose health risks upon exposure. Overall, this compound is significant in synthetic organic chemistry due to its versatile reactivity and potential applications in various fields.

ethyl 2-(chloromethyl)-1,3-oxazole-4-carboxylate

68683-09-0: Ethyl 2-(chloromethyl)-1,3-oxazole-4-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 carboxylate group, which contributes to its acidity and reactivity, and a chloromethyl substituent that enhances its electrophilic properties, making it useful in various chemical reactions. Ethyl 2-(chloromethyl)-1,3-oxazole-4-carboxylate is typically a colorless to pale yellow liquid or solid, depending on its purity and specific conditions. It is soluble in organic solvents, which facilitates its use in organic synthesis. The presence of the chloromethyl group allows for further functionalization, making it a valuable intermediate in the synthesis of pharmaceuticals and agrochemicals. Safety data indicates that it should be handled with care, as it may pose health risks upon exposure. Overall, this compound is significant in synthetic organic chemistry due to its versatile reactivity and potential applications in various fields.

CAS 68683-09-0

ethyl 2-(chloromethyl)-1,3-oxazole-4-carboxylate

ethyl 2-(chloromethyl)-1,3-oxazole-4-carboxylate

Ref: 10-F522367