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CAS 98708-79-3

:

4-(1-Methylethyl)phenylalanine

Description:
4-(1-Methylethyl)phenylalanine, also known as a derivative of phenylalanine, is an amino acid characterized by the presence of a branched alkyl group at the para position of the phenyl ring. This compound features a chiral center, which contributes to its potential biological activity and interactions. It is typically classified as a non-polar, hydrophobic amino acid due to the isopropyl group attached to the phenyl ring, influencing its solubility and reactivity in various environments. The presence of the amino group (-NH2) and carboxylic acid group (-COOH) allows it to participate in peptide bond formation, making it relevant in protein synthesis. Its structural modifications can affect its role in metabolic pathways and its interactions with enzymes and receptors. As a synthetic amino acid, it may be utilized in research and pharmaceutical applications, particularly in the study of protein structure and function, as well as in the development of novel therapeutic agents.
Formula:C12H17NO2
InChI:InChI=1S/C12H17NO2/c1-8(2)10-5-3-9(4-6-10)7-11(13)12(14)15/h3-6,8,11H,7,13H2,1-2H3,(H,14,15)
InChI key:InChIKey=CYHRSNOITZHLJN-UHFFFAOYSA-N
SMILES:C(C(C(O)=O)N)C1=CC=C(C(C)C)C=C1
Synonyms:
  • 2-Amino-3-(4-isopropylphenyl)propanoic acid
  • 2-Amino-3-[4-(propan-2-yl)phenyl]propanoic acid
  • 4-(1-Methylethyl)phenylalanine
  • <span class="text-smallcaps">DL</span>-Phenylalanine, 4-(1-methylethyl)-
  • <span class="text-smallcaps">DL</span>-p-Isopropylphenylalanine
  • DL-Phenylalanine, 4-(1-methylethyl)-
  • Phenylalanine, 4-(1-methylethyl)-
  • DL-p-Isopropylphenylalanine
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