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CAS 1452518-88-5

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2-Thiophenecarboxylic acid, 4,5-diamino-, methyl ester, hydrochloride (1:2)

Description:
2-Thiophenecarboxylic acid, 4,5-diamino-, methyl ester, hydrochloride (1:2) is a chemical compound characterized by its thiophene ring structure, which contributes to its aromatic properties and potential reactivity. The presence of carboxylic acid and amino groups indicates that it can participate in various chemical reactions, including esterification and amination. As a hydrochloride salt, it is typically more soluble in water compared to its free base form, enhancing its utility in biological and pharmaceutical applications. The methyl ester group suggests that it may exhibit ester-like behavior, potentially influencing its reactivity and interaction with biological systems. This compound may be of interest in medicinal chemistry due to its structural features, which could be relevant for drug design or synthesis. Its specific properties, such as melting point, solubility, and biological activity, would need to be determined through experimental studies. Overall, this compound represents a versatile building block in organic synthesis and may have applications in various fields, including pharmaceuticals and agrochemicals.
Formula:C6H8N2O2S·2ClH
InChI:InChI=1S/C6H8N2O2S.2ClH/c1-10-6(9)4-2-3(7)5(8)11-4;;/h2H,7-8H2,1H3;2*1H
InChI key:InChIKey=YDLQRAQFZCQSQT-UHFFFAOYSA-N
SMILES:C(OC)(=O)C1=CC(N)=C(N)S1.Cl
Synonyms:
  • 2-Thiophenecarboxylic acid, 4,5-diamino-, methyl ester, hydrochloride (1:2)
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