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CAS 155239-51-3

:

(2S)-Amino(2,3-dihydro-1H-inden-2-yl)acetic acid

Description:
(2S)-Amino(2,3-dihydro-1H-inden-2-yl)acetic acid, also known by its CAS number 155239-51-3, is an amino acid derivative characterized by its unique bicyclic structure, which includes a dihydroindene moiety. This compound features an amino group and a carboxylic acid functional group, typical of amino acids, which contributes to its potential biological activity. The stereochemistry indicated by the (2S) designation suggests that it has a specific spatial arrangement, which can influence its interactions with biological systems, particularly in terms of receptor binding and enzymatic activity. The presence of the indene structure may also impart unique properties, such as increased lipophilicity or specific binding affinities. This compound is of interest in medicinal chemistry and pharmacology, as modifications to amino acids can lead to the development of novel therapeutics. Its solubility, stability, and reactivity would depend on the surrounding conditions, including pH and temperature, which are critical for its application in various chemical and biological contexts.
Formula:C11H13NO2
InChI:InChI=1S/C11H13NO2/c12-10(11(13)14)9-5-7-3-1-2-4-8(7)6-9/h1-4,9-10H,5-6,12H2,(H,13,14)/t10-/m0/s1
InChI key:InChIKey=GUDHMDVRURNAHL-JTQLQIEISA-N
SMILES:[C@H](C(O)=O)(N)C1CC=2C(C1)=CC=CC2
Synonyms:
  • (S)-2-Amino-2-(2,3-dihydro-1H-inden-2-yl)acetic acid
  • 1H-Indene-2-acetic acid, α-amino-2,3-dihydro-, (αS)-
  • L-(2-Indanyl)glycine
  • 1H-Indene-2-acetic acid, α-amino-2,3-dihydro-, (S)-
  • (αS)-α-Amino-2,3-dihydro-1H-indene-2-acetic acid
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