CAS 25796-04-7
:2-amino-3-(4-bromo-1H-indol-3-yl)propanoic acid
Description:
2-amino-3-(4-bromo-1H-indol-3-yl)propanoic acid, also known by its CAS number 25796-04-7, is an amino acid derivative characterized by the presence of an indole ring and a bromine substituent. This compound features a propanoic acid backbone with an amino group at one end and a brominated indole moiety at the other, which contributes to its unique chemical properties. The indole structure is known for its aromaticity and ability to participate in various chemical reactions, making this compound potentially interesting for pharmaceutical applications. The bromine atom introduces additional reactivity and can influence the compound's biological activity, solubility, and stability. As an amino acid derivative, it may exhibit properties typical of amino acids, such as being zwitterionic in nature at physiological pH. This compound's specific interactions, including potential binding to biological targets, would depend on its three-dimensional conformation and the electronic effects of the bromine substituent. Overall, 2-amino-3-(4-bromo-1H-indol-3-yl)propanoic acid represents a complex structure with potential implications in medicinal chemistry and biochemistry.
Formula:C11H11BrN2O2
Synonyms:- 4-Bromotryptophan
- Dl-4-Bromotryptophan
- 4-Bromo-DL-tryptophan
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Found 3 products.
2-Amino-3-(4-bromo-1H-indol-3-yl)propanoic acid
CAS:Formula:C11H11BrN2O2Purity:97%Molecular weight:283.125


