Ethyl 2-amino-4,5-dimethylthiophene-3-carboxylate

≥95%

Reagent Code: #181902
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CAS Number 4815-24-1

science Other reagents with same CAS 4815-24-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 199.27 g/mol
Formula C₉H₁₃NO₂S
badge Registry Numbers
MDL Number MFCD00085051
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Storage Room temperature

description Product Description

Widely used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds with potential anti-inflammatory, antimicrobial, and anticancer properties. Its structure serves as a building block for heterocyclic compounds, enabling the construction of complex thiophene-based molecules. Commonly employed in medicinal chemistry for scaffold modification and structure-activity relationship studies. Also utilized in agrochemical research for designing new pesticides and herbicides due to its favorable reactivity and stability. Frequently applied in combinatorial chemistry and high-throughput screening protocols to generate diverse compound libraries.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿148.50
inventory 5g
10-20 days ฿600.00
inventory 25g
10-20 days ฿2,780.00
inventory 100g
10-20 days ฿11,110.00
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Ethyl 2-amino-4,5-dimethylthiophene-3-carboxylate
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Widely used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds with potential anti-inflammatory, antimicrobial, and anticancer properties. Its structure serves as a building block for heterocyclic compounds, enabling the construction of complex thiophene-based molecules. Commonly employed in medicinal chemistry for scaffold modification and structure-activity relationship studies. Also utilized in agrochemical research for designing

Widely used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds with potential anti-inflammatory, antimicrobial, and anticancer properties. Its structure serves as a building block for heterocyclic compounds, enabling the construction of complex thiophene-based molecules. Commonly employed in medicinal chemistry for scaffold modification and structure-activity relationship studies. Also utilized in agrochemical research for designing new pesticides and herbicides due to its favorable reactivity and stability. Frequently applied in combinatorial chemistry and high-throughput screening protocols to generate diverse compound libraries.

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