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CAS 55720-26-8

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(S)-trans-2-Amino-4-(2-aminoethoxy)-3-butenoic acid hydrochloride

Description:
(S)-trans-2-Amino-4-(2-aminoethoxy)-3-butenoic acid hydrochloride, commonly referred to as a derivative of amino acids, is characterized by its structural features that include an amino group, a butenoic acid backbone, and an ethoxy side chain. This compound is typically a white to off-white crystalline powder, soluble in water due to the presence of the hydrochloride salt form, which enhances its solubility and stability. It exhibits properties typical of amino acids, such as the ability to participate in peptide bond formation and act as a building block for proteins. The specific stereochemistry indicated by the "(S)" designation suggests that it has a particular spatial arrangement that can influence its biological activity and interactions. This compound may have applications in biochemical research, particularly in studies related to neurotransmitter synthesis or as a potential therapeutic agent. As with many amino acid derivatives, it is important to handle it with care, following appropriate safety protocols in laboratory settings.
Formula:C6H12N2O3·ClH
InChI:InChI=1S/C6H12N2O3.ClH/c7-2-4-11-3-1-5(8)6(9)10;/h1,3,5H,2,4,7-8H2,(H,9,10);1H/b3-1+;/t5-;/m0./s1
InChI key:InChIKey=ZDCPLYVEFATMJF-BTIOQYSDSA-N
SMILES:[C@H](/C=C/OCCN)(C(O)=O)N.Cl
Synonyms:
  • (S)-trans-2-Amino-4-(2-aminoethoxy)-3-butenoic acid hydrochloride
  • 3-Butenoic acid, 2-amino-4-(2-aminoethoxy)-, hydrochloride (1:1), (2S,3E)-
  • 3-Butenoic acid, 2-amino-4-(2-aminoethoxy)-, monohydrochloride, (2S,3E)-
  • 3-Butenoic acid, 2-amino-4-(2-aminoethoxy)-, monohydrochloride, [S-(E)]-
  • 55720-26-8
  • 55720-26-8 {Hydrochloride}
  • <span class="text-smallcaps">L</span>-2-Amino-4-(2′-aminoethoxy)-trans-3-butenoic acid hydrochloride
  • Abg 3168
  • Aviglycine hydrochloride
  • ReTain
  • See more synonyms
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