CAS 4815-38-7
:Ethyl 2-amino-4-methyl-5-phenylthiophene-3-carboxylate
Description:
Ethyl 2-amino-4-methyl-5-phenylthiophene-3-carboxylate, with CAS number 4815-38-7, is a chemical compound that belongs to the class of thiophene derivatives. This compound features a thiophene ring, which is a five-membered aromatic heterocycle containing sulfur, and is substituted with an ethyl ester group, an amino group, a methyl group, and a phenyl group. The presence of these functional groups contributes to its potential biological activity and reactivity. Ethyl 2-amino-4-methyl-5-phenylthiophene-3-carboxylate is typically characterized by its solid state at room temperature, and it may exhibit moderate solubility in organic solvents. The compound's structure suggests it may participate in various chemical reactions, including nucleophilic substitutions and coupling reactions, making it of interest in synthetic organic chemistry. Additionally, its unique combination of functional groups may impart specific pharmacological properties, warranting further investigation in medicinal chemistry and drug development.
Formula:C14H15NO2S
InChI:InChI=1S/C14H15NO2S/c1-3-17-14(16)11-9(2)12(18-13(11)15)10-7-5-4-6-8-10/h4-8H,3,15H2,1-2H3
InChI key:InChIKey=FXPVOLWQNNGFHA-UHFFFAOYSA-N
SMILES:CC1=C(SC(N)=C1C(OCC)=O)C2=CC=CC=C2
Synonyms:- 2-Amino-4-methyl-5-phenyl-thiophene-3-carboxylic acid ethyl ester
- 2-Amino-4-methyl-5-phenylthiophene-3-carboxylic acid ethyl ester
- 3-Thiophenecarboxylic acid, 2-amino-4-methyl-5-phenyl-, ethyl ester
- T5Sj Bz Cvo2 D1 Er [Wln]
- Ethyl 2-amino-4-methyl-5-phenylthiophene-3-carboxylate
- Ethyl 2-amino-4-methyl-5-phenylthiophene-3-carboxylate
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Found 5 products.
ETHYL 2-AMINO-4-METHYL-5-PHENYLTHIOPHENE-3-CARBOXYLATE
CAS:Formula:C14H15NO2SPurity:95%Molecular weight:261.3394ETHYL 2-AMINO-4-METHYL-5-PHENYLTHIOPHENE-3-CARBOXYLATE
CAS:ETHYL 2-AMINO-4-METHYL-5-PHENYLTHIOPHENE-3-CARBOXYLATEPurity:≥98%Molecular weight:261.34g/molEthyl 2-amino-4-methyl-5-phenylthiophene-3-carboxylate
CAS:<p>Ethyl 2-amino-4-methyl-5-phenylthiophene-3-carboxylate</p>Purity:≥95%Molecular weight:261.34g/molETHYL 2-AMINO-4-METHYL-5-PHENYLTHIOPHENE-3-CARBOXYLATE
CAS:<p>ETHYL 2-AMINO-4-METHYL-5-PHENYLTHIOPHENE-3-CARBOXYLATE targets the prostaglandin E2 receptor EP2 subtype (human)</p>Formula:C14H15NO2SPurity:99.98%Color and Shape:SolidMolecular weight:261.34Ethyl 2-amino-4-methyl-5-phenylthiophene-3-carboxylate
CAS:<p>This drug is a potent inhibitor of the glutamate receptor. It binds to the glutamate receptor and blocks the binding of glutamate, which is an excitatory neurotransmitter in the central nervous system. Ethyl 2-amino-4-methyl-5-phenylthiophene-3-carboxylate can be used as an antagonist to inhibit glutamate activity, thereby preventing neuronal death in patients with Parkinson's disease and Alzheimer's disease. This drug also has an antagonistic effect on leukocyte elastase, which is a protein that breaks down connective tissue and cartilage. The synthesizing of pyrimidines is inhibited by this drug. It also inhibits receptors for glutamate, specifically N-methyl D-aspartate (NMDA) receptors. This drug blocks the binding of NMDA to its receptor site, preventing ion channels from opening so neurons cannot fire or release neurotransmitters.</p>Formula:C14H15NO2SPurity:Min. 95%Molecular weight:261.34 g/mol



