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CAS 54260-89-8

:

2-Propenoic acid, 3-(1H-imidazol-5-yl)-, methyl ester, hydrochloride (1:1), (2E)-

Description:
2-Propenoic acid, 3-(1H-imidazol-5-yl)-, methyl ester, hydrochloride (1:1), (2E)-, commonly referred to as a derivative of acrylic acid, features a propenoic acid backbone with an imidazole ring substitution. This compound is characterized by its ability to participate in various chemical reactions due to the presence of both the carboxylic acid and the imidazole functional groups. The methyl ester form enhances its solubility in organic solvents, making it useful in various applications, including pharmaceuticals and biochemistry. The hydrochloride salt form indicates that it is a stable, ionic compound, which can improve its handling and storage properties. This compound may exhibit biological activity, potentially acting as a ligand or a precursor in synthetic pathways. Its structural features suggest it could be involved in polymerization processes or serve as a building block for more complex molecules. As with many chemical substances, safety precautions should be observed when handling, as it may pose health risks depending on exposure levels.
Formula:C7H9ClN2O2
InChI:InChI=1/C7H8N2O2.ClH/c1-11-7(10)3-2-6-4-8-5-9-6;/h2-5H,1H3,(H,8,9);1H/b3-2+;
InChI key:InChIKey=ZCBDROJOIVNJSB-SQQVDAMQSA-N
SMILES:C(=C/C(OC)=O)\C1=CN=CN1.Cl
Synonyms:
  • 2-Propenoic acid, 3-(1H-imidazol-4-yl)-, methyl ester, monohydrochloride, (E)-
  • methyl (2E)-3-(1H-imidazol-5-yl)prop-2-enoate hydrochloride
  • Methyl (E)-3-(1H-imidazol-4-yl)acrylate monohydrochloride
  • 2-Propenoic acid, 3-(1H-imidazol-5-yl)-, methyl ester, hydrochloride (1:1), (2E)-
  • 2-Propenoic acid, 3-(1H-imidazol-4-yl)-, methyl ester, monohydrochloride, (2E)-
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