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CAS 610300-07-7

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(3S,5R)-3-Amino-5-methyloctanoic acid

Description:
(3S,5R)-3-Amino-5-methyloctanoic acid, with the CAS number 610300-07-7, is a chiral amino acid characterized by its specific stereochemistry at the 3 and 5 positions. This compound features an aliphatic chain, which contributes to its hydrophobic properties, while the amino and carboxylic acid functional groups impart polar characteristics, allowing for potential interactions in biological systems. The presence of a methyl group at the 5 position enhances its steric bulk, influencing its reactivity and interactions with enzymes or receptors. As an amino acid, it plays a role in protein synthesis and may be involved in various metabolic pathways. Its unique stereochemistry may also affect its biological activity, making it of interest in pharmaceutical research and development. Additionally, the compound's solubility and stability can vary depending on environmental conditions such as pH and temperature, which are important factors to consider in applications involving this amino acid.
Formula:C9H19NO2
InChI:InChI=1S/C9H19NO2/c1-3-4-7(2)5-8(10)6-9(11)12/h7-8H,3-6,10H2,1-2H3,(H,11,12)/t7-,8+/m1/s1
InChI key:InChIKey=JXEHXYFSIOYTAH-SFYZADRCSA-N
SMILES:C([C@@H](CC(O)=O)N)[C@@H](CCC)C
Synonyms:
  • Octanoic acid, 3-amino-5-methyl-, (3S,5R)-
  • PD 0332334
  • (3S,5R)-3-Amino-5-methyloctanoic acid
  • Imagabalin
  • PF 00195889
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