Ethyl 2-bromo-5-chlorothiazole-4-carboxylate

98%

Reagent Code: #181918
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CAS Number 425392-44-5

science Other reagents with same CAS 425392-44-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 270.53 g/mol
Formula C₆H₅BrClNO₂S
badge Registry Numbers
MDL Number MFCD08704625
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Widely used as an intermediate in the synthesis of agrochemicals, particularly insecticides and fungicides. Its structure allows for easy modification, making it valuable in developing active ingredients that target specific pests or pathogens. Commonly employed in the production of neonicotinoid-like compounds due to the reactivity of the bromo and chloro substituents, enabling coupling reactions and functional group transformations. Also utilized in medicinal chemistry for constructing heterocyclic systems with biological activity. Its ester group facilitates further chain elongation or cyclization in multi-step syntheses. Preferred in industrial processes for its stability and predictable reaction behavior under various conditions.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,370.00
inventory 1g
10-20 days ฿3,710.00
inventory 10g
10-20 days ฿32,080.00
inventory 5g
10-20 days ฿18,460.00
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Ethyl 2-bromo-5-chlorothiazole-4-carboxylate
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Widely used as an intermediate in the synthesis of agrochemicals, particularly insecticides and fungicides. Its structure allows for easy modification, making it valuable in developing active ingredients that target specific pests or pathogens. Commonly employed in the production of neonicotinoid-like compounds due to the reactivity of the bromo and chloro substituents, enabling coupling reactions and functional group transformations. Also utilized in medicinal chemistry for constructing heterocyclic system
Widely used as an intermediate in the synthesis of agrochemicals, particularly insecticides and fungicides. Its structure allows for easy modification, making it valuable in developing active ingredients that target specific pests or pathogens. Commonly employed in the production of neonicotinoid-like compounds due to the reactivity of the bromo and chloro substituents, enabling coupling reactions and functional group transformations. Also utilized in medicinal chemistry for constructing heterocyclic systems with biological activity. Its ester group facilitates further chain elongation or cyclization in multi-step syntheses. Preferred in industrial processes for its stability and predictable reaction behavior under various conditions.
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