(S)-2-Formamido-3-(4-hydroxy-3,5-diiodophenyl)propanoic acid, with the CAS number 906327-16-0, is a chemical compound characterized by its specific stereochemistry and functional groups. It features a propanoic acid backbone, which is a three-carbon carboxylic acid, and includes a formamido group (-NHCHO) that contributes to its reactivity and solubility. The presence of a 4-hydroxy-3,5-diiodophenyl moiety indicates that the compound has significant iodine substitution on the aromatic ring, which can influence its biological activity and chemical properties. The hydroxyl group (-OH) enhances its potential for hydrogen bonding, affecting solubility in polar solvents. This compound may exhibit interesting pharmacological properties due to its structural features, making it a subject of interest in medicinal chemistry. Its specific stereochemistry, denoted by the (S) configuration, suggests that it may interact differently with biological targets compared to its enantiomer. Overall, this compound's unique structure positions it as a potentially valuable molecule in research and development.

(S)-2-ForMaMido-3-(4-hydroxy-3,5-diiodophenyl)propanoic Acid

906327-16-0: (S)-2-Formamido-3-(4-hydroxy-3,5-diiodophenyl)propanoic acid, with the CAS number 906327-16-0, is a chemical compound characterized by its specific stereochemistry and functional groups. It features a propanoic acid backbone, which is a three-carbon carboxylic acid, and includes a formamido group (-NHCHO) that contributes to its reactivity and solubility. The presence of a 4-hydroxy-3,5-diiodophenyl moiety indicates that the compound has significant iodine substitution on the aromatic ring, which can influence its biological activity and chemical properties. The hydroxyl group (-OH) enhances its potential for hydrogen bonding, affecting solubility in polar solvents. This compound may exhibit interesting pharmacological properties due to its structural features, making it a subject of interest in medicinal chemistry. Its specific stereochemistry, denoted by the (S) configuration, suggests that it may interact differently with biological targets compared to its enantiomer. Overall, this compound's unique structure positions it as a potentially valuable molecule in research and development.

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CAS 906327-16-0

(S)-2-ForMaMido-3-(4-hydroxy-3,5-diiodophenyl)propanoic Acid

N-Formyl-3,5-diiodo-L-tyrosine

Ref: 3D-GLB32716