Methyl 3-formylfuran-2-carboxylate, with the CAS number 28921-39-3, is an organic compound characterized by its furan ring structure, which is a five-membered aromatic ring containing oxygen. This compound features a formyl group (-CHO) and a carboxylate group (-COOCH3) attached to the furan ring, contributing to its reactivity and potential applications in organic synthesis. It is typically a colorless to pale yellow liquid or solid, depending on its purity and form. Methyl 3-formylfuran-2-carboxylate is known for its role in various chemical reactions, including condensation and cycloaddition reactions, making it valuable in the synthesis of more complex organic molecules. Its functional groups allow for further derivatization, enhancing its utility in medicinal chemistry and materials science. Additionally, it may exhibit biological activity, although specific biological properties would require further investigation. Proper handling and storage are essential due to its potential reactivity and the need for safety precautions in laboratory settings.

methyl 3-formylfuran-2-carboxylate

28921-39-3: Methyl 3-formylfuran-2-carboxylate, with the CAS number 28921-39-3, is an organic compound characterized by its furan ring structure, which is a five-membered aromatic ring containing oxygen. This compound features a formyl group (-CHO) and a carboxylate group (-COOCH3) attached to the furan ring, contributing to its reactivity and potential applications in organic synthesis. It is typically a colorless to pale yellow liquid or solid, depending on its purity and form. Methyl 3-formylfuran-2-carboxylate is known for its role in various chemical reactions, including condensation and cycloaddition reactions, making it valuable in the synthesis of more complex organic molecules. Its functional groups allow for further derivatization, enhancing its utility in medicinal chemistry and materials science. Additionally, it may exhibit biological activity, although specific biological properties would require further investigation. Proper handling and storage are essential due to its potential reactivity and the need for safety precautions in laboratory settings.

Methyl 3-formylfuran-2-carboxylate

<p>Methyl 3-formylfuran-2-carboxylate is a selective, triethyl, acrylates, carbonyl groups, phosphite, chloride, carbonyl, diisopropyl, phosphonates, fluoride, potassium and phosphites. It reacts with isomeric hydroxyphosphonates.</p>

CAS 28921-39-3

methyl 3-formylfuran-2-carboxylate

Methyl 3-formylfuran-2-carboxylate

Ref: IN-DA002X2R

Methyl 3-formylfuran-2-carboxylate

Ref: 3D-DBA92139