The chemical substance known as {(3-fluorophenyl)carbonyl}aminoacetate, with the CAS number 366-47-2, is an organic compound characterized by the presence of a 3-fluorophenyl group attached to a carbonyl moiety, which is further linked to an aminoacetate functional group. This compound typically exhibits properties associated with both aromatic and amine functionalities, contributing to its potential reactivity and solubility in various solvents. The fluorine atom in the 3-position of the phenyl ring can influence the electronic properties of the molecule, potentially enhancing its reactivity or altering its interaction with biological targets. The aminoacetate portion suggests that the compound may participate in hydrogen bonding and could be involved in various biochemical processes. Its structural features may also indicate potential applications in pharmaceuticals or agrochemicals, where such derivatives are often explored for their biological activity. Overall, the compound's characteristics are defined by its functional groups, molecular structure, and the presence of the fluorine substituent, which collectively influence its chemical behavior and potential applications.

{[(3-fluorophenyl)carbonyl]amino}acetate

366-47-2: The chemical substance known as {(3-fluorophenyl)carbonyl}aminoacetate, with the CAS number 366-47-2, is an organic compound characterized by the presence of a 3-fluorophenyl group attached to a carbonyl moiety, which is further linked to an aminoacetate functional group. This compound typically exhibits properties associated with both aromatic and amine functionalities, contributing to its potential reactivity and solubility in various solvents. The fluorine atom in the 3-position of the phenyl ring can influence the electronic properties of the molecule, potentially enhancing its reactivity or altering its interaction with biological targets. The aminoacetate portion suggests that the compound may participate in hydrogen bonding and could be involved in various biochemical processes. Its structural features may also indicate potential applications in pharmaceuticals or agrochemicals, where such derivatives are often explored for their biological activity. Overall, the compound's characteristics are defined by its functional groups, molecular structure, and the presence of the fluorine substituent, which collectively influence its chemical behavior and potential applications.

CAS 366-47-2

{[(3-fluorophenyl)carbonyl]amino}acetate

(3-Fluoro-benzoylamino)-acetic acid

Ref: IN-DA00CLNG

(3-Fluoro-benzoylamino)-acetic acid

Ref: 54-PC909034