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CAS 1676-73-9

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γ-Benzyl L-glutamate

Description:
γ-Benzyl L-glutamate, with the CAS number 1676-73-9, is an amino acid derivative that features a benzyl group attached to the gamma position of L-glutamic acid. This compound is characterized by its white crystalline appearance and is soluble in polar organic solvents. It exhibits properties typical of amino acids, including the ability to participate in peptide bond formation, making it relevant in peptide synthesis and biochemistry. The presence of the benzyl group enhances its hydrophobic character, which can influence its interactions in biological systems and its utility in drug design. γ-Benzyl L-glutamate is often used as a protecting group in organic synthesis, particularly in the synthesis of peptides, due to its stability under various reaction conditions. Additionally, it can serve as a building block in the development of pharmaceuticals and other bioactive compounds. Its structural features contribute to its reactivity and functionality in various chemical reactions, making it a valuable compound in both research and industrial applications.
Formula:C12H15NO4
InChI:InChI=1S/C12H15NO4/c13-10(12(15)16)6-7-11(14)17-8-9-4-2-1-3-5-9/h1-5,10H,6-8,13H2,(H,15,16)/t10-/m0/s1
InChI key:InChIKey=BGGHCRNCRWQABU-JTQLQIEISA-N
SMILES:C(OC(CC[C@@H](C(O)=O)N)=O)C1=CC=CC=C1
Synonyms:
  • (2S)-2-Amino-5-(benzyloxy)-5-oxopentanoic acid
  • (2S)-2-Azaniumyl-5-oxo-5-phenylmethoxypentanoate
  • (2S)-2-amino-5-(benzyloxy)-5-oxopentanoic acid (non-preferred name)
  • (2S,4R)-2-ammonio-4-benzylpentanedioate
  • (S)-2-Amino-5-(benzyloxy)-5-oxopentanoic acid
  • 2-Amino-5-(Benzyloxy)-5-Oxopentanoic Acid (Non-Preferred Name)
  • 5-Benzyl <span class="text-smallcaps">L</span>-glutamate
  • <span class="text-smallcaps">L</span>-Glutamate-γ-benzyl ester
  • <span class="text-smallcaps">L</span>-Glutamic acid 5-benzyl ester
  • <span class="text-smallcaps">L</span>-Glutamic acid γ-benzyl ester
  • See more synonyms
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