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CAS 16856-13-6

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L-Aspartic acid, 4-methyl ester, hydrochloride (1:1)

Description:
L-Aspartic acid, 4-methyl ester, hydrochloride (1:1) is a derivative of the amino acid L-aspartic acid, characterized by the presence of a methyl ester group at the 4-position of the aspartic acid backbone. This compound is typically encountered as a white crystalline powder and is soluble in water, which is a common trait for many amino acid derivatives. The hydrochloride form indicates that it is a salt formed with hydrochloric acid, enhancing its stability and solubility in aqueous solutions. L-Aspartic acid itself plays a crucial role in various biological processes, including protein synthesis and neurotransmission. The methyl ester modification can influence its reactivity and bioavailability, making it of interest in biochemical research and potential pharmaceutical applications. As with many amino acid derivatives, it may exhibit specific optical activity due to the presence of chiral centers, which is significant in the context of biological activity. Safety data should be consulted for handling and usage, as with all chemical substances.
Formula:C5H9NO4·ClH
InChI:InChI=1S/C5H9NO4.ClH/c1-10-4(7)2-3(6)5(8)9;/h3H,2,6H2,1H3,(H,8,9);1H/t3-;/m0./s1
InChI key:InChIKey=QRBMPUYOGOCYDJ-DFWYDOINSA-N
SMILES:C([C@@H](C(O)=O)N)C(OC)=O.Cl
Synonyms:
  • (2S)-2-amino-4-methoxy-4-oxobutanoic acid (non-preferred name)
  • (2S)-2-amino-4-methoxy-4-oxobutanoic acid hydrochloride (non-preferred name)
  • (S)-2-Amino-4-methoxy-4-oxobutanoic acid hydrochloride
  • 2-Amino-4-Methoxy-4-Oxobutanoic Acid (Non-Preferred Name)
  • <span class="text-smallcaps">L</span>-Aspartic acid β-methyl ester hydrochloride
  • <span class="text-smallcaps">L</span>-Aspartic acid, 4-methyl ester, hydrochloride
  • <span class="text-smallcaps">L</span>-Aspartic acid, 4-methyl ester, hydrochloride (1:1)
  • Aspartic acid(ome)-OH HCl
  • Aspartic acid, 4-methyl ester, hydrochloride, <span class="text-smallcaps">L</span>-
  • H-Asp(OMe)-OH.HCl
  • See more synonyms
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