CAS 31891-06-2
:2-Amino-thiophene-3-carboxylic acid ethyl ester
Description:
2-Amino-thiophene-3-carboxylic acid ethyl ester is an organic compound characterized by its thiophene ring structure, which is a five-membered aromatic heterocycle containing sulfur. This compound features an amino group (-NH2) and an ethyl ester functional group, contributing to its reactivity and potential applications in organic synthesis. The presence of the carboxylic acid moiety, in the form of an ethyl ester, enhances its solubility in organic solvents, making it useful in various chemical reactions. The compound is typically a solid at room temperature and may exhibit moderate stability under standard conditions. Its unique structure allows for potential applications in pharmaceuticals, agrochemicals, and as intermediates in the synthesis of more complex molecules. Additionally, the amino group can participate in hydrogen bonding, influencing its physical properties and reactivity. Overall, 2-Amino-thiophene-3-carboxylic acid ethyl ester is a versatile compound with significant implications in synthetic organic chemistry.
Formula:C7H9NO2S
InChI:InChI=1/C7H9NO2S/c1-2-10-7(9)5-3-4-11-6(5)8/h3-4H,2,8H2,1H3
SMILES:CCOC(=O)c1ccsc1N
Synonyms:- Ethyl 2-aminothiophene-3-carboxylate
- 2-Aminothiophene-3-Carboxylic Acid Ethyl Ester
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Found 6 products.
Ethyl 2-aminothiophene-3-carboxylate, 97%
CAS:<p>Ethyl 2-aminothiophene-3-carboxylate is used as an organic chemical synthesis intermediate. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product </p>Formula:C7H9NO2SPurity:97%Color and Shape:Low melt solid or viscous liquid, BlackMolecular weight:171.213-Thiophenecarboxylic acid, 2-amino-, ethyl ester
CAS:Formula:C7H9NO2SPurity:97%Color and Shape:SolidMolecular weight:171.2169Ethyl 2-aminothiophene-3-carboxylate
CAS:<p>Ethyl 2-aminothiophene-3-carboxylate</p>Purity:97%Color and Shape:SolidMolecular weight:171.22g/molEthyl 2-Aminothiophene-3-carboxylate
CAS:Controlled Product<p>Applications Ethyl 2-Aminothiophene-3-carboxylate (cas# 31891-06-2) is a compound useful in organic synthesis.<br></p>Formula:C7H9NO2SColor and Shape:NeatMolecular weight:171.22Ethyl 2-aminothiophene-3-carboxylate
CAS:<p>Ethyl 2-aminothiophene-3-carboxylate is a triazole derivative with anticancer activity. It has been shown to inhibit the adenosine A1 receptor and show anticancer activity in vitro. The drug has also been shown to have potent cytotoxic effects against cancer cells, which may be due to its ability to activate apoptosis in tumor cells through structural modifications that lead to the inhibition of DNA synthesis. This compound has also been shown to be less toxic than other chemotherapeutic drugs, such as thiosemicarbazide and ethylene diamine, and it does not cause red blood cell lysis or hemolysis.</p>Formula:C7H9NO2SPurity:Min. 95%Color and Shape:Slightly Yellow PowderMolecular weight:171.22 g/molEthyl 2-aminothiophene-3-carboxylate
CAS:Formula:C7H9NO2SPurity:97%Color and Shape:SolidMolecular weight:171.21





