Ethyl 6-bromobenzo[b]thiophene-3-carboxylate

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Reagent Code: #184403
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CAS Number 946427-88-9

science Other reagents with same CAS 946427-88-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 285.16 g/mol
Formula C₁₁H₉BrO₂S
badge Registry Numbers
MDL Number MFCD28501951
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of anticoagulant and anti-inflammatory agents. Its structure allows for selective functionalization, making it valuable in constructing complex heterocyclic systems found in bioactive molecules. Commonly employed in cross-coupling reactions such as Suzuki and Heck reactions to form carbon-carbon bonds in drug discovery programs. Also utilized in the preparation of organic semiconductors due to the electron-rich nature of the benzothiophene core, contributing to materials with enhanced charge transport properties.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,420.00
inventory 1g
10-20 days ฿6,220.00
inventory 5g
10-20 days ฿22,550.00

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Ethyl 6-bromobenzo[b]thiophene-3-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of anticoagulant and anti-inflammatory agents. Its structure allows for selective functionalization, making it valuable in constructing complex heterocyclic systems found in bioactive molecules. Commonly employed in cross-coupling reactions such as Suzuki and Heck reactions to form carbon-carbon bonds in drug discovery programs. Also utilized in the preparation of organic semiconductors due to the electron-ric

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of anticoagulant and anti-inflammatory agents. Its structure allows for selective functionalization, making it valuable in constructing complex heterocyclic systems found in bioactive molecules. Commonly employed in cross-coupling reactions such as Suzuki and Heck reactions to form carbon-carbon bonds in drug discovery programs. Also utilized in the preparation of organic semiconductors due to the electron-rich nature of the benzothiophene core, contributing to materials with enhanced charge transport properties.

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