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4815-38-7

Ethyl 2-amino-4-methyl-5-phenylthiophene-3-carboxylate

Catalog#: AR00DJCJ  |   CAS#: 4815-38-7  |   MDL#: MFCD00652592  |   MF: C14H15NO2S  |   MW: 261.3394

Packsize Purity Price Availability Quantity
1mg 95% $54.00 Global Stock Buy Now Add To Cart
5mg 95% $107.00 Global Stock Buy Now Add To Cart
10mg 95% $149.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00DJCJ
Chemical Name Ethyl 2-amino-4-methyl-5-phenylthiophene-3-carboxylate
CAS Number 4815-38-7
Molecular Formula C14H15NO2S
Molecular Weight 261.3394
MDL Number MFCD00652592
SMILES CCOC(=O)c1c(N)sc(c1C)c1ccccc1

Ethyl 2-amino-4-methyl-5-phenylthiophene-3-carboxylate is a versatile compound widely utilized in chemical synthesis for the development of novel pharmaceuticals, agrochemicals, and materials. Due to its unique structural features, this compound serves as a key intermediate in the synthesis of various biologically active molecules.One of the primary applications of Ethyl 2-amino-4-methyl-5-phenylthiophene-3-carboxylate is in the design and synthesis of organic molecules with specific pharmacological properties. By incorporating this compound into the molecular structure, medicinal chemists can modulate the bioactivity, metabolic stability, and pharmacokinetic profile of potential drug candidates. This strategic use of Ethyl 2-amino-4-methyl-5-phenylthiophene-3-carboxylate allows for the creation of new therapeutic agents with improved efficacy and reduced side effects.Furthermore, in agrochemical research, the synthesis of novel pesticides and herbicides often requires the construction of complex molecular frameworks. Ethyl 2-amino-4-methyl-5-phenylthiophene-3-carboxylate serves as a valuable building block for the introduction of functional groups that contribute to the desired biological activity of these agricultural chemicals. By leveraging the synthetic versatility of this compound, chemists can access a diverse range of pesticide and herbicide analogs with enhanced performance and environmental safety profiles.In addition to its pharmaceutical and agrochemical applications, Ethyl 2-amino-4-methyl-5-phenylthiophene-3-carboxylate finds utility in the synthesis of advanced materials with tailored properties. By incorporating this compound into the polymer backbone or functionalizing its side chains, materials scientists can engineer polymers, oligomers, or small molecules with specific electronic, optical, or mechanical characteristics. This flexibility in molecular design enables the development of high-performance materials for applications in electronics, optoelectronics, and organic photovoltaics.Overall, Ethyl 2-amino-4-methyl-5-phenylthiophene-3-carboxylate plays a crucial role in chemical synthesis by enabling the construction of diverse molecular architectures with targeted functionalities. Its applicability across pharmaceutical, agrochemical, and material science domains underscores its importance as a valuable building block for the creation of innovative compounds and materials.
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GHS Pictogram N/A
UN# N/A
Hazard Statements -
Class N/A
Packing Group N/A

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