Ethyl-4-methyl-3,5-oxazolecarboxylate, with the CAS number 76284-27-0, is an organic compound characterized by its oxazole ring structure, which is a five-membered heterocyclic compound containing both nitrogen and oxygen atoms. This substance typically appears as a colorless to pale yellow liquid or solid, depending on its purity and specific conditions. It is known for its role as an intermediate in organic synthesis, particularly in the preparation of various pharmaceuticals and agrochemicals. The presence of the ethyl ester functional group contributes to its reactivity, allowing for further chemical modifications. Ethyl-4-methyl-3,5-oxazolecarboxylate is generally soluble in organic solvents, such as ethanol and dichloromethane, but may have limited solubility in water. Safety data indicates that, like many organic compounds, it should be handled with care, using appropriate personal protective equipment to avoid inhalation or skin contact. Overall, its unique structure and reactivity make it a valuable compound in synthetic organic chemistry.

ETHYL-4-METHYL-3,5-OXAZOLECARBOXYLATE

76284-27-0: Ethyl-4-methyl-3,5-oxazolecarboxylate, with the CAS number 76284-27-0, is an organic compound characterized by its oxazole ring structure, which is a five-membered heterocyclic compound containing both nitrogen and oxygen atoms. This substance typically appears as a colorless to pale yellow liquid or solid, depending on its purity and specific conditions. It is known for its role as an intermediate in organic synthesis, particularly in the preparation of various pharmaceuticals and agrochemicals. The presence of the ethyl ester functional group contributes to its reactivity, allowing for further chemical modifications. Ethyl-4-methyl-3,5-oxazolecarboxylate is generally soluble in organic solvents, such as ethanol and dichloromethane, but may have limited solubility in water. Safety data indicates that, like many organic compounds, it should be handled with care, using appropriate personal protective equipment to avoid inhalation or skin contact. Overall, its unique structure and reactivity make it a valuable compound in synthetic organic chemistry.

CAS 76284-27-0

ETHYL-4-METHYL-3,5-OXAZOLECARBOXYLATE

Ethyl 2-methyloxazole-5-carboxylate

Ref: IN-DA00G2AJ