Methyl 2-amino-5-(2-fluorophenyl)-1,3-thiazole-4-carboxylate

≥95%

Reagent Code: #214254
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CAS Number 886361-38-2

science Other reagents with same CAS 886361-38-2

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scatter_plot Molecular Information
Weight 252.27 g/mol
Formula C₁₁H₉FN₂O₂S
badge Registry Numbers
MDL Number MFCD06200924
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, light-proof

description Product Description

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders, anti-inflammatory agents, infectious diseases, and cancer therapeutics. Featuring a 1,3-thiazole core with a 2-fluorophenyl substituent and methyl carboxylate ester, its structure enhances inhibition of target enzymes, supporting the development of kinase inhibitors and antimicrobial candidates. Commonly employed in medicinal chemistry for scaffold modification in drug discovery programs. Also utilized in agrochemical research for designing novel pesticides with improved selectivity.

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inventory 1mg
10-20 days ฿5,990.00

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Methyl 2-amino-5-(2-fluorophenyl)-1,3-thiazole-4-carboxylate
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Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders, anti-inflammatory agents, infectious diseases, and cancer therapeutics. Featuring a 1,3-thiazole core with a 2-fluorophenyl substituent and methyl carboxylate ester, its structure enhances inhibition of target enzymes, supporting the development of kinase inhibitors and antimicrobial candidates. Commonly employed in medicinal chemistry for scaffold modi

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders, anti-inflammatory agents, infectious diseases, and cancer therapeutics. Featuring a 1,3-thiazole core with a 2-fluorophenyl substituent and methyl carboxylate ester, its structure enhances inhibition of target enzymes, supporting the development of kinase inhibitors and antimicrobial candidates. Commonly employed in medicinal chemistry for scaffold modification in drug discovery programs. Also utilized in agrochemical research for designing novel pesticides with improved selectivity.

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