4-Bromo-2-thiophenecarboxylic Acid

98%

Reagent Code: #144778
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CAS Number 16694-18-1

science Other reagents with same CAS 16694-18-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 207.04 g/mol
Formula C₅H₃BrO₂S
badge Registry Numbers
MDL Number MFCD03422294
thermostat Physical Properties
Melting Point 120.0 to 124.0 deg-C
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of thiophene-based bioactive molecules. Its bromine functionality allows for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex organic frameworks. Commonly employed in the preparation of antihypertensive agents, antiviral compounds, and functional materials. Also utilized in the design of organic semiconductors and conjugated polymers due to the electron-rich nature of the thiophene ring.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿168.00
5g
10-20 days ฿174.00
25g
10-20 days ฿1,240.00
100g
10-20 days ฿4,950.00
4-Bromo-2-thiophenecarboxylic Acid
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of thiophene-based bioactive molecules. Its bromine functionality allows for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex organic frameworks. Commonly employed in the preparation of antihypertensive agents, antiviral compounds, and functional materials. Also utilized in the design of organic semiconductors and conjugated polymers due to the

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of thiophene-based bioactive molecules. Its bromine functionality allows for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex organic frameworks. Commonly employed in the preparation of antihypertensive agents, antiviral compounds, and functional materials. Also utilized in the design of organic semiconductors and conjugated polymers due to the electron-rich nature of the thiophene ring.

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