Ethyl 2-(4-bromophenyl)thiazole-4-carboxylate

≥95%

Reagent Code: #181971
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CAS Number 885278-75-1

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Weight 312.18 g/mol
Formula C₁₂H₁₀BrNO₂S
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MDL Number MFCD06738340
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules with potential antitumor, antimicrobial, and anti-inflammatory properties. Its structure supports derivatization for use in medicinal chemistry research, especially in creating libraries of thiazole-based compounds for drug discovery. Also employed in the preparation of organic semiconductors and fluorescent materials due to the electron-accepting nature of the thiazole ring and the bromine handle for cross-coupling reactions.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,050.00
inventory 5g
10-20 days ฿10,970.00
inventory 25g
10-20 days ฿45,660.00
inventory 250mg
10-20 days ฿1,230.00

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Ethyl 2-(4-bromophenyl)thiazole-4-carboxylate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules with potential antitumor, antimicrobial, and anti-inflammatory properties. Its structure supports derivatization for use in medicinal chemistry research, especially in creating libraries of thiazole-based compounds for drug discovery. Also employed in the preparation of organic semiconductors and fluorescent materials due to the electron-accepting nature of the thiazole ring and th

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules with potential antitumor, antimicrobial, and anti-inflammatory properties. Its structure supports derivatization for use in medicinal chemistry research, especially in creating libraries of thiazole-based compounds for drug discovery. Also employed in the preparation of organic semiconductors and fluorescent materials due to the electron-accepting nature of the thiazole ring and the bromine handle for cross-coupling reactions.

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