Methyl 5-{[(chloroacetyl)amino]methyl}furan-2-carboxylate is a synthetic organic compound characterized by its furan ring structure, which is a five-membered aromatic ring containing oxygen. This compound features a methyl ester functional group, contributing to its solubility in organic solvents. The presence of a chloroacetyl group indicates that it has potential reactivity, particularly in nucleophilic substitution reactions. The amino group attached to the chloroacetyl moiety suggests that this compound may participate in various chemical transformations, including acylation and amide formation. Its structure implies potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the furan ring's biological activity. The compound's molecular interactions may also be influenced by the presence of the ester and amine functionalities, which can engage in hydrogen bonding and other intermolecular forces. Overall, methyl 5-{[(chloroacetyl)amino]methyl}furan-2-carboxylate is a versatile compound with potential utility in various chemical and biological applications.

methyl 5-{[(chloroacetyl)amino]methyl}furan-2-carboxylate

345991-81-3: 2-Furancarboxylic Acid, 5-[[(2-Chloroacetyl)Amino]Methyl]-, Methyl Ester, Methyl 5-{[(chloroacetyl)amino]methyl}-2-furoate

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CAS 345991-81-3: methyl 5-{[(chloroacetyl)amino]methyl}furan-2-carboxylate

Methyl 5-{[(chloroacetyl)amino]methyl}-2-furoate

Ref: 3D-FM131760

methyl 5-{[(chloroacetyl)amino]methyl}-2-furoate

Ref: IN-DA00C5SZ