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CAS 78213-60-2

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(2S)-amino(1-methylcyclopropyl)ethanoic acid

Description:
(2S)-Amino(1-methylcyclopropyl)ethanoic acid, also known as a derivative of amino acids, is characterized by its unique cyclopropyl structure, which contributes to its distinct chemical properties. This compound features a chiral center, making it optically active, and it exists predominantly in the S configuration. The presence of the amino group (-NH2) and the carboxylic acid group (-COOH) classifies it as an amino acid, which plays a crucial role in biological systems, particularly in protein synthesis. The cyclopropyl group introduces strain and rigidity to the molecule, potentially influencing its reactivity and interactions with biological targets. This compound may exhibit specific pharmacological properties, making it of interest in medicinal chemistry. Its solubility in water and organic solvents can vary, depending on the pH and the presence of other functional groups. Overall, (2S)-amino(1-methylcyclopropyl)ethanoic acid represents a fascinating example of how structural features can impact the behavior and utility of amino acid derivatives in various chemical and biological contexts.
Formula:C6H11NO2
InChI:InChI=1/C6H11NO2/c1-6(2-3-6)4(7)5(8)9/h4H,2-3,7H2,1H3,(H,8,9)/t4-/m1/s1
SMILES:CC1(CC1)[C@@H](C(=O)O)N
Synonyms:
  • (2S)-2-amino-2-(1-methylcyclopropyl)acetic acid hydrochloride
  • Cyclopropaneacetic acid, α-aMino-1-Methyl-, (αS)- hydrochloride
  • (2S)-Amino-2-(1-methylcyclopropyl)acetic acid
  • Cyclopropaneacetic acid, alpha-amino-1-methyl-, (alpha S)- hydrochloride
  • (S)-2-amino-2-(1-methylcyclopropyl)acetic acid hydrochloride
  • (S)-2-Amino-2-(1-methylcyclopropyl)acetic acid
  • Cyclopropaneacetic acid, α-amino-1-methyl-, (αS)-
  • (αS)-α-Amino-1-methylcyclopropaneacetic acid
  • PA-4046I
  • See more synonyms
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