1H-Indole-3-butanoic acid, α-(acetylamino)-, with the CAS number 205813-00-9, is a chemical compound that belongs to the class of indole derivatives. It features an indole ring, which is a bicyclic structure composed of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring. The compound is characterized by the presence of a butanoic acid side chain and an acetylamino group, which contributes to its potential biological activity. This compound may exhibit properties relevant to plant growth regulation, as indole derivatives are often associated with auxin activity, influencing processes such as cell elongation and division. Additionally, the acetylamino substitution can enhance solubility and bioavailability. The compound's structure suggests it may participate in various chemical reactions, including acylation and amide formation, making it of interest in synthetic organic chemistry and potential pharmaceutical applications. As with many indole derivatives, it may also exhibit interesting pharmacological properties, warranting further investigation into its biological effects and mechanisms of action.

1H-Indole-3-butanoicacid, a-(acetylamino)-

205813-00-9: 1H-Indole-3-butanoic acid, α-(acetylamino)-, with the CAS number 205813-00-9, is a chemical compound that belongs to the class of indole derivatives. It features an indole ring, which is a bicyclic structure composed of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring. The compound is characterized by the presence of a butanoic acid side chain and an acetylamino group, which contributes to its potential biological activity. This compound may exhibit properties relevant to plant growth regulation, as indole derivatives are often associated with auxin activity, influencing processes such as cell elongation and division. Additionally, the acetylamino substitution can enhance solubility and bioavailability. The compound's structure suggests it may participate in various chemical reactions, including acylation and amide formation, making it of interest in synthetic organic chemistry and potential pharmaceutical applications. As with many indole derivatives, it may also exhibit interesting pharmacological properties, warranting further investigation into its biological effects and mechanisms of action.

N-Acetyl-D,L-homotryptophan

<p>Applications N-Acetyl-D,L-homotryptophan (cas# 205813-00-9) is a compound useful in organic synthesis.<br>References J. Am. Chem. Soc., 70, 1962 (1948)<br></p>

CAS 205813-00-9

1H-Indole-3-butanoicacid, a-(acetylamino)-

N-Acetyl-D,L-homotryptophan

Ref: 7W-GM9884

N-Acetyl-D,L-homotryptophan

Ref: 54-OR7840T

N-Acetyl-D,L-homotryptophan

Ref: TR-A178400