5-Bromothiophene-3-carboxamide

96%

Reagent Code: #145308
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CAS Number 189329-94-0

science Other reagents with same CAS 189329-94-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 206.06 g/mol
Formula C₅H₄BrNOS
thermostat Physical Properties
Boiling Point 304.0±27.0°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in pharmaceutical synthesis as an intermediate for developing bioactive molecules, particularly in the production of thiophene-based drugs with potential antitumor, antimicrobial, and anti-inflammatory properties. Its bromine functionality allows for cross-coupling reactions, making it valuable in medicinal chemistry for building complex organic structures. Also employed in the development of organic semiconductors due to the electron-rich nature of the thiophene ring, contributing to materials used in optoelectronic devices.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿820.00
inventory 250mg
10-20 days ฿2,470.00
inventory 1g
10-20 days ฿6,380.00
inventory 5g
10-20 days ฿23,540.00

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5-Bromothiophene-3-carboxamide
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Used in pharmaceutical synthesis as an intermediate for developing bioactive molecules, particularly in the production of thiophene-based drugs with potential antitumor, antimicrobial, and anti-inflammatory properties. Its bromine functionality allows for cross-coupling reactions, making it valuable in medicinal chemistry for building complex organic structures. Also employed in the development of organic semiconductors due to the electron-rich nature of the thiophene ring, contributing to materials used

Used in pharmaceutical synthesis as an intermediate for developing bioactive molecules, particularly in the production of thiophene-based drugs with potential antitumor, antimicrobial, and anti-inflammatory properties. Its bromine functionality allows for cross-coupling reactions, making it valuable in medicinal chemistry for building complex organic structures. Also employed in the development of organic semiconductors due to the electron-rich nature of the thiophene ring, contributing to materials used in optoelectronic devices.

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