The chemical substance known as (2R)-2-{[(4-fluorophenyl)sulfonyl]amino}propanoate, with the CAS number 780-97-2, is an organic compound characterized by its specific structural features. It contains a propanoate backbone, which is a three-carbon chain with a carboxylate functional group. The presence of a sulfonamide group, specifically a sulfonyl moiety attached to a 4-fluorophenyl ring, contributes to its chemical reactivity and potential biological activity. The fluorine atom on the phenyl ring can influence the compound's electronic properties and lipophilicity, potentially affecting its pharmacokinetics and interactions with biological targets. This compound may exhibit properties typical of sulfonamides, such as antibacterial activity, although its specific applications would depend on further research. Additionally, the stereochemistry indicated by the (2R) designation suggests that it has a specific spatial arrangement, which can be crucial for its biological function and interaction with enzymes or receptors. Overall, this compound represents a class of molecules that may have significant implications in medicinal chemistry and drug development.

(2R)-2-{[(4-fluorophenyl)sulfonyl]amino}propanoate

780-97-2: The chemical substance known as (2R)-2-{[(4-fluorophenyl)sulfonyl]amino}propanoate, with the CAS number 780-97-2, is an organic compound characterized by its specific structural features. It contains a propanoate backbone, which is a three-carbon chain with a carboxylate functional group. The presence of a sulfonamide group, specifically a sulfonyl moiety attached to a 4-fluorophenyl ring, contributes to its chemical reactivity and potential biological activity. The fluorine atom on the phenyl ring can influence the compound's electronic properties and lipophilicity, potentially affecting its pharmacokinetics and interactions with biological targets. This compound may exhibit properties typical of sulfonamides, such as antibacterial activity, although its specific applications would depend on further research. Additionally, the stereochemistry indicated by the (2R) designation suggests that it has a specific spatial arrangement, which can be crucial for its biological function and interaction with enzymes or receptors. Overall, this compound represents a class of molecules that may have significant implications in medicinal chemistry and drug development.

CAS 780-97-2

(2R)-2-{[(4-fluorophenyl)sulfonyl]amino}propanoate

2-([(4-Fluorophenyl)sulfonyl]amino)propanoic acid

Ref: IN-DA00G30V

2-(4-Fluorobenzenesulphamido)propanoic acid

Ref: 54-PC9378

2-{[(4-Fluorophenyl)sulfonyl]amino}propanoic acid

Ref: 10-F010120