Ethyl 2-(2-bromothiazol-4-yl)acetate

95%

Reagent Code: #185302
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CAS Number 56355-79-4

science Other reagents with same CAS 56355-79-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 250.11 g/mol
Formula C₇H₈BrNO₂S
badge Registry Numbers
MDL Number MFCD18413040
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Widely used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of thiazole-based drugs which exhibit antimicrobial, antifungal, and anti-inflammatory activities. It plays a key role in constructing more complex heterocyclic systems due to the reactivity of the bromine atom and the ester functionality, enabling coupling reactions and further functionalization. Commonly employed in agrochemical research for designing novel pesticides and herbicides, thanks to the bioactive nature of thiazole derivatives. Its structure allows for easy modification, making it valuable in medicinal chemistry for structure-activity relationship (SAR) studies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,200.00
inventory 250mg
10-20 days ฿4,210.00
inventory 5g
10-20 days ฿61,090.00
inventory 1g
10-20 days ฿14,960.00

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Ethyl 2-(2-bromothiazol-4-yl)acetate
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Widely used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of thiazole-based drugs which exhibit antimicrobial, antifungal, and anti-inflammatory activities. It plays a key role in constructing more complex heterocyclic systems due to the reactivity of the bromine atom and the ester functionality, enabling coupling reactions and further functionalization. Commonly employed in agrochemical research for designing novel pesticides and herbicides, thanks to the bioact

Widely used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of thiazole-based drugs which exhibit antimicrobial, antifungal, and anti-inflammatory activities. It plays a key role in constructing more complex heterocyclic systems due to the reactivity of the bromine atom and the ester functionality, enabling coupling reactions and further functionalization. Commonly employed in agrochemical research for designing novel pesticides and herbicides, thanks to the bioactive nature of thiazole derivatives. Its structure allows for easy modification, making it valuable in medicinal chemistry for structure-activity relationship (SAR) studies.

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