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Atomfair Methyl 3-amino-5-phenylthiophene-2-carboxylate C12H11NO2S
Description Methyl 3-amino-5-phenylthiophene-2-carboxylate (CAS No. 100063-22-7) is a high-purity organic compound with the molecular formula C12H11NO2S . This thiophene derivative features a phenyl substituent at the 5-position and an amino group at the 3-position, making it a versatile intermediate for pharmaceutical and materials science research. Its methyl ester functionality enhances solubility in organic solvents, facilitating reactions such as amidation, hydrolysis, or further functionalization. With a molecular weight of 233.29 g/mol , this compound is supplied as a crystalline solid, rigorously tested for purity via HPLC, NMR, and mass spectrometry. Ideal for heterocyclic chemistry, drug discovery, and ligand synthesis, it is…
Description
Description
Methyl 3-amino-5-phenylthiophene-2-carboxylate (CAS No. 100063-22-7) is a high-purity organic compound with the molecular formula C12H11NO2S. This thiophene derivative features a phenyl substituent at the 5-position and an amino group at the 3-position, making it a versatile intermediate for pharmaceutical and materials science research. Its methyl ester functionality enhances solubility in organic solvents, facilitating reactions such as amidation, hydrolysis, or further functionalization. With a molecular weight of 233.29 g/mol, this compound is supplied as a crystalline solid, rigorously tested for purity via HPLC, NMR, and mass spectrometry. Ideal for heterocyclic chemistry, drug discovery, and ligand synthesis, it is packaged under inert conditions to ensure stability and longevity.
- CAS No: 100063-22-7
- Molecular Formula: C12H11NO2S
- Molecular Weight: 233.29
- Exact Mass: 233.05104977
- Monoisotopic Mass: 233.05104977
- IUPAC Name: methyl 3-amino-5-phenylthiophene-2-carboxylate
- SMILES: COC(=O)C1=C(C=C(S1)C2=CC=CC=C2)N
- Synonyms: methyl 3-amino-5-phenylthiophene-2-carboxylate, 100063-22-7, DTXSID70351450, DTXCID00302516, 640-912-1
Application
Methyl 3-amino-5-phenylthiophene-2-carboxylate serves as a key building block in medicinal chemistry for the synthesis of bioactive thiophene scaffolds. Researchers utilize it in the development of kinase inhibitors, antimicrobial agents, and CNS-targeted compounds due to its rigid aromatic core. Its reactive amino group enables conjugation with carboxylic acids or electrophiles, while the ester allows for late-stage diversification. This compound is also employed in materials science for constructing ??-conjugated systems in organic electronics.
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