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CAS 35761-27-4

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L-Alanine, 3-amino-N-[(phenylmethoxy)carbonyl]-, methyl ester, hydrochloride (1:1)

Description:
L-Alanine, 3-amino-N-[(phenylmethoxy)carbonyl]-, methyl ester, hydrochloride (1:1), with the CAS number 35761-27-4, is a derivative of the amino acid L-alanine. This compound features a methyl ester functional group, which enhances its solubility and bioavailability. The presence of the phenylmethoxycarbonyl group contributes to its stability and may influence its interaction with biological systems. As a hydrochloride salt, it is typically more soluble in water compared to its free base form, making it suitable for various applications in pharmaceuticals and biochemistry. The compound exhibits characteristics typical of amino acids, including the ability to participate in peptide bond formation, and it may serve as a building block in the synthesis of peptides or other biologically active molecules. Its specific stereochemistry, being an L-amino acid, is crucial for its biological activity, particularly in protein synthesis. Overall, this compound is of interest in medicinal chemistry and research involving amino acid derivatives.
Formula:C12H16N2O4·ClH
InChI:InChI=1S/C12H16N2O4.ClH/c1-17-11(15)10(7-13)14-12(16)18-8-9-5-3-2-4-6-9;/h2-6,10H,7-8,13H2,1H3,(H,14,16);1H/t10-;/m0./s1
InChI key:InChIKey=OLOFLUKZNNTGBC-PPHPATTJSA-N
SMILES:C(OC(N[C@H](C(OC)=O)CN)=O)C1=CC=CC=C1.Cl
Synonyms:
  • 3-Amino-N-(benzyloxycarbonyl)-L-alanine methyl ester hydrochloride
  • L-Alanine, 3-amino-N-[(phenylmethoxy)carbonyl]-, methyl ester, hydrochloride (1:1)
  • L-Alanine, 3-amino-N-[(phenylmethoxy)carbonyl]-, methyl ester, monohydrochloride
  • (2S)-2-[[(Benzyloxy)carbonyl]amino]-3-methoxy-3-oxopropan-1-aminium chloride
  • (S)-Methyl 3-amino-2-(benzyloxycarbonylamino)propionate hydrochloride
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