Ethyl 4-amino-2-(methylthio)thiazole-5-carboxylate

95%

Reagent Code: #181914
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CAS Number 39736-29-3

science Other reagents with same CAS 39736-29-3

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scatter_plot Molecular Information
Weight 218.30 g/mol
Formula C₇H₁₀N₂O₂S₂
badge Registry Numbers
MDL Number MFCD01830310
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Widely used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of thiazole-based drugs with antimicrobial, antifungal, and anti-inflammatory properties. It serves as a building block in the development of sulfonamide antibiotics due to its reactive amino and ester functional groups, which allow for easy modification and derivatization. Commonly employed in the preparation of kinase inhibitors and other bioactive molecules in medicinal chemistry research. Also utilized in agrochemicals for the development of crop protection agents owing to its structural stability and reactivity. Its methylthio group enhances lipophilicity, improving cell membrane permeability in drug design. Frequently used in combinatorial chemistry and high-throughput screening for lead compound optimization.

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿28,500.00
inventory 250mg
10-20 days ฿572.00
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Ethyl 4-amino-2-(methylthio)thiazole-5-carboxylate
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Widely used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of thiazole-based drugs with antimicrobial, antifungal, and anti-inflammatory properties. It serves as a building block in the development of sulfonamide antibiotics due to its reactive amino and ester functional groups, which allow for easy modification and derivatization. Commonly employed in the preparation of kinase inhibitors and other bioactive molecules in medicinal chemistry research. Also utiliz

Widely used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of thiazole-based drugs with antimicrobial, antifungal, and anti-inflammatory properties. It serves as a building block in the development of sulfonamide antibiotics due to its reactive amino and ester functional groups, which allow for easy modification and derivatization. Commonly employed in the preparation of kinase inhibitors and other bioactive molecules in medicinal chemistry research. Also utilized in agrochemicals for the development of crop protection agents owing to its structural stability and reactivity. Its methylthio group enhances lipophilicity, improving cell membrane permeability in drug design. Frequently used in combinatorial chemistry and high-throughput screening for lead compound optimization.

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