Ethyl 5-bromo-2-phenylthiazole-4-carboxylate

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Reagent Code: #183699
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CAS Number 914347-21-0

science Other reagents with same CAS 914347-21-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 312.18 g/mol
Formula C₁₂H₁₀BrNO₂S
badge Registry Numbers
MDL Number MFCD08275710
thermostat Physical Properties
Boiling Point 408°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry seal

description Product Description

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals and agrochemicals. Its structure supports the development of kinase inhibitors and antimicrobial agents. Commonly employed in medicinal chemistry for constructing thiazole-based drug candidates due to its reactivity and ability to undergo palladium-catalyzed cross-coupling reactions. Also utilized in research settings to design novel compounds with potential anticancer and anti-inflammatory properties.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,060.00
inventory 1g
10-20 days ฿4,120.00
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Ethyl 5-bromo-2-phenylthiazole-4-carboxylate
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Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals and agrochemicals. Its structure supports the development of kinase inhibitors and antimicrobial agents. Commonly employed in medicinal chemistry for constructing thiazole-based drug candidates due to its reactivity and ability to undergo palladium-catalyzed cross-coupling reactions. Also utilized in research settings to design novel compounds with potential anticancer and anti-inflammatory prope

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals and agrochemicals. Its structure supports the development of kinase inhibitors and antimicrobial agents. Commonly employed in medicinal chemistry for constructing thiazole-based drug candidates due to its reactivity and ability to undergo palladium-catalyzed cross-coupling reactions. Also utilized in research settings to design novel compounds with potential anticancer and anti-inflammatory properties.

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