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CAS 125089-02-3

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Methyl 3-amino-4,5-dihydro-4-methyl-2-thiophenecarboxylate

Description:
Methyl 3-amino-4,5-dihydro-4-methyl-2-thiophenecarboxylate, with the CAS number 125089-02-3, is an organic compound characterized by its thiophene ring structure, which contributes to its unique chemical properties. This compound features an amino group, which can participate in various chemical reactions, making it a potential candidate for applications in pharmaceuticals and organic synthesis. The presence of the methyl groups enhances its hydrophobic characteristics, influencing its solubility and reactivity. Additionally, the dihydro form indicates that it has a saturated structure, which may affect its stability and interaction with other molecules. The carboxylate group suggests that it can act as an acid or a base, depending on the pH of the environment. Overall, this compound's structural features make it interesting for further research in medicinal chemistry and materials science, where its reactivity and functional groups can be exploited for the development of new compounds or materials.
Formula:C7H11NO2S
InChI:InChI=1S/C7H11NO2S/c1-4-3-11-6(5(4)8)7(9)10-2/h4H,3,8H2,1-2H3
InChI key:InChIKey=KHUBACFPTYUTGI-UHFFFAOYSA-N
SMILES:C(OC)(=O)C1=C(N)C(C)CS1
Synonyms:
  • 2-Thiophenecarboxylic acid, 3-amino-4,5-dihydro-4-methyl-, methyl ester
  • 3-Amino-2-carbomethoxy-4-methyl-4,5-dihydrothiophene
  • 3-Amino-4,5-dihydro-4-methyl-2-Thiophenecarboxylic acid methyl ester
  • Methyl 3-Amino-4-Methyl-4,5-Dihydrothiophene-2-Carboxylate
  • Methyl 3-amino-4,5-dihydro-4-methyl-2-thiophenecarboxylate
  • Methyl 4-Methyl-3-Amino-4,5-Dihydrothiophene-2-Carboxylate
  • Methyl 4-Methyl-3-Aminodihydrothiophene-2-Carbonate
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