CymitQuimica logo

CAS 57224-50-7

:

(2S)-2-Amino-4,4-dimethylpentanoic acid

Description:
(2S)-2-Amino-4,4-dimethylpentanoic acid, commonly known as a derivative of amino acids, is characterized by its chiral center at the second carbon, which contributes to its specific stereochemistry. This compound features an amino group (-NH2) and a carboxylic acid group (-COOH), typical of amino acids, making it a zwitterionic species at physiological pH. The presence of two methyl groups on the fourth carbon enhances its hydrophobic characteristics, influencing its solubility and interaction with biological systems. This compound is often studied for its potential applications in pharmaceuticals and biochemistry, particularly in the context of protein synthesis and metabolic pathways. Its molecular structure allows it to participate in various biochemical reactions, and its chirality can affect its biological activity and interactions with enzymes and receptors. As with many amino acid derivatives, it may exhibit unique properties in terms of stability, reactivity, and interaction with other biomolecules, making it a subject of interest in both synthetic and medicinal chemistry.
Formula:C7H15NO2
InChI:InChI=1S/C7H15NO2/c1-7(2,3)4-5(8)6(9)10/h5H,4,8H2,1-3H3,(H,9,10)/t5-/m0/s1
InChI key:InChIKey=LPBSHGLDBQBSPI-YFKPBYRVSA-N
SMILES:[C@H](CC(C)(C)C)(C(O)=O)N
Synonyms:
  • (2S)-2-Amino-4,4-dimethylpentanoic acid
  • 3-tert-Butyl-<span class="text-smallcaps">L</span>-alanine
  • 4-Methyl-<span class="text-smallcaps">L</span>-leucine
  • 4-methyl-L-leucine
  • <span class="text-smallcaps">L</span>-2-Amino-4,4-dimethylpentanoic acid
  • <span class="text-smallcaps">L</span>-Leucine, 4-methyl-
  • <span class="text-smallcaps">L</span>-γ-Methylleucine
  • H-.beta.-tBu-Ala-OH
  • Pentanoic acid, 2-amino-4,4-dimethyl-, (2S)-
  • γ-Methyl-<span class="text-smallcaps">L</span>-leucine
  • See more synonyms
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 10 products.