CAS 22288-78-4
:Methyl 3-aminothiophene-2-carboxylate
Description:
Methyl 3-aminothiophene-2-carboxylate is an organic compound characterized by its thiophene ring, which is a five-membered aromatic heterocycle containing sulfur. This compound features an amino group (-NH2) and a carboxylate group (-COOCH3) attached to the thiophene ring, contributing to its reactivity and potential applications in various chemical reactions. The presence of the amino group allows for the formation of hydrogen bonds, enhancing its solubility in polar solvents. Methyl 3-aminothiophene-2-carboxylate is often utilized in the synthesis of pharmaceuticals and agrochemicals due to its ability to participate in electrophilic substitution reactions and its role as a building block in organic synthesis. Additionally, the compound may exhibit biological activity, making it of interest in medicinal chemistry. Its molecular structure and functional groups contribute to its unique properties, influencing its behavior in chemical reactions and interactions with other substances. Safety data should be consulted for handling and usage, as with any chemical compound.
Formula:C6H7NO2S
InChI:InChI=1S/C6H7NO2S/c1-9-6(8)5-4(7)2-3-10-5/h2-3H,7H2,1H3
InChI key:InChIKey=TWEQNZZOOFKOER-UHFFFAOYSA-N
SMILES:C(OC)(=O)C1=C(N)C=CS1
Synonyms:- 2-Aminothiophene-3-carboxylic acid methyl ester
- 2-Thiophenecarboxylic acid, 3-amino-, methyl ester
- 3-Amino-2-methoxycarbonylthiophene
- 3-Amino-2-thiophene methyl formate
- 3-Amino-2-thiophenecarboxylic acid methyl ester
- 3-Aminothiophen-2-carboxylic acid methyl ester
- 3-Aminothiophene-2-carboxylic acid methyl ester
- Methyl 3-amino-2-thenoate
- Methyl 3-amino-2-thiophene carboxylate ester
- Methyl 3-amino-2-thiophenecarboxylate
- Methyl 3-aminothiophene-2-carboxylate
- Thiofuran amine
- See more synonyms
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Found 7 products.
Methyl 3-Amino-2-thiophenecarboxylate
CAS:Formula:C6H7NO2SPurity:>98.0%(GC)(T)Color and Shape:White to Gray to Brown powder to crystalMolecular weight:157.19Methyl 3-aminothiophene-2-carboxylate, 98+%
CAS:<p>Methyl 3-aminothiophene-2-carboxylate is used in the synthesis of 4-nitro and 4-aminothienyl ureas, total synthesis of quinazolinocarboline alkaloids and in preparation of thienopyrimidinone analogs. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfo</p>Formula:C6H7NO2SPurity:98+%Color and Shape:Crystals or powder or crystalline powder, Cream to pale brownMolecular weight:157.19Methyl 3-amino-2-thiophenecarboxylate
CAS:Formula:C6H7NO2SPurity:98%Color and Shape:SolidMolecular weight:157.1903Methyl 3-aminothiophene-2-carboxylate
CAS:<p>Methyl 3-aminothiophene-2-carboxylate</p>Formula:C6H7NO2SPurity:≥95%Color and Shape: brown solidMolecular weight:157.19027g/molMethyl 3-aminothiophene-2-carboxylate
CAS:Formula:C6H7NO2SPurity:97%Color and Shape:SolidMolecular weight:157.193-Amino-2-thiophenecarboxylic acid methyl ester
CAS:<p>3-Amino-2-thiophenecarboxylic acid methyl ester is a replication inhibitor that targets hydroxyl groups in the mitochondrial membrane. It has been shown to induce a decrease in the mitochondrial membrane potential, leading to a loss of cell viability and an increase in locomotor activity. 3-Amino-2-thiophenecarboxylic acid methyl ester also induces apoptosis by inhibiting the expression of cyclin D1 and Bcl-XL proteins, which are key regulators of cancer cell proliferation. 3-Amino-2-thiophenecarboxylic acid methyl ester is able to inhibit cancer cell growth in vitro, which may be due to its ability to inhibit h3 acetylation and MDA-MB231 cell proliferation. 3-Amino-2-thiophenecarboxylic acid methyl ester also has antiinflammatory effects by modulating inflammation pathways such as NFκB signaling.</p>Formula:C6H7NO2SPurity:Min. 95%Color and Shape:PowderMolecular weight:157.19 g/mol






