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CAS 367278-49-7

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(R)-3-Amino-4,4-dimethylpentanoic acid

Description:
(R)-3-Amino-4,4-dimethylpentanoic acid, also known as a derivative of amino acids, is characterized by its chiral center, which contributes to its specific optical activity. This compound features an amino group (-NH2) and a carboxylic acid group (-COOH), typical of amino acids, making it a potential building block for peptides and proteins. The presence of two methyl groups on the fourth carbon enhances its steric bulk, influencing its interactions and solubility in various solvents. This compound is often studied for its potential applications in pharmaceuticals, particularly in the development of neuroprotective agents or as a precursor in synthetic pathways. Its unique structure may also affect its biological activity, making it of interest in medicinal chemistry. Additionally, the specific stereochemistry (R configuration) can significantly impact its biological properties and interactions with enzymes or receptors. Overall, (R)-3-Amino-4,4-dimethylpentanoic acid represents a fascinating subject for research in both organic and medicinal chemistry.
Formula:C7H15NO2
InChI:InChI=1S/C7H15NO2/c1-7(2,3)5(8)4-6(9)10/h5H,4,8H2,1-3H3,(H,9,10)/t5-/m1/s1
InChI key:InChIKey=MIMSUZKTGRXZNZ-RXMQYKEDSA-N
SMILES:[C@@H](CC(O)=O)(C(C)(C)C)N
Synonyms:
  • (3R)-3-Amino-4,4-dimethylpentanoic acid
  • Pentanoic acid, 3-amino-4,4-dimethyl-, (3R)-
  • (R)-3-amino-4,4-dimethylpentanoic acid
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