Ethyl 5-Bromo-4-Methylthiophene-2-Carboxylate

97%

Reagent Code: #185464
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CAS Number 186521-81-3

science Other reagents with same CAS 186521-81-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 249.12 g/mol
Formula C₈H₉BrO₂S
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of thiophene-based active ingredients. Its functional groups enable coupling reactions, making it valuable in medicinal chemistry for constructing heterocyclic compounds. Commonly employed in the preparation of kinase inhibitors and anti-inflammatory agents. Also utilized in materials science for creating conductive polymers and organic semiconductors due to the thiophene backbone’s electron-rich properties.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿1,710.00
250mg
10-20 days ฿2,800.00
1g
10-20 days ฿5,600.00
5g
10-20 days ฿18,790.00
10g
10-20 days ฿26,830.00
Ethyl 5-Bromo-4-Methylthiophene-2-Carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of thiophene-based active ingredients. Its functional groups enable coupling reactions, making it valuable in medicinal chemistry for constructing heterocyclic compounds. Commonly employed in the preparation of kinase inhibitors and anti-inflammatory agents. Also utilized in materials science for creating conductive polymers and organic semiconductors due to the thiophene backbone’s electron-

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of thiophene-based active ingredients. Its functional groups enable coupling reactions, making it valuable in medicinal chemistry for constructing heterocyclic compounds. Commonly employed in the preparation of kinase inhibitors and anti-inflammatory agents. Also utilized in materials science for creating conductive polymers and organic semiconductors due to the thiophene backbone’s electron-rich properties.

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