5-Formyl-2-thiopheneboronic acid

97%

Reagent Code: #90929
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Alias 5-formyl-2-thiophene boronic acid ;5-formylthiophene-2-boronic acid, 5-formylthiophene-2-boronic acid
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CAS Number 4347-33-5

science Other reagents with same CAS 4347-33-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 155.97 g/mol
Formula C₅H₅BO₃S
badge Registry Numbers
MDL Number MFCD02093666
thermostat Physical Properties
Melting Point 132-135 °C(lit.)
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for creating complex organic molecules, especially in the pharmaceutical industry where it aids in the development of drug candidates. The formyl group on the thiophene ring allows for further functionalization, making it versatile in designing molecules with specific properties. Additionally, it finds application in material science for synthesizing conjugated polymers and organic electronic materials, which are essential in the production of organic light-emitting diodes (OLEDs) and other advanced materials. Its boronic acid moiety enables efficient cross-coupling with aryl halides, facilitating the construction of carbon-carbon bonds in a controlled manner.

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Test Parameter Specification
Purity (Neutralization Titration) 96.5-103.5%
Appearance Yellow to orange to brown powder or crystals
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿550.00
inventory 5g
10-20 days ฿1,550.00
inventory 25g
10-20 days ฿5,860.00
inventory 100g
10-20 days ฿22,700.00

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5-Formyl-2-thiopheneboronic acid
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This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for creating complex organic molecules, especially in the pharmaceutical industry where it aids in the development of drug candidates. The formyl group on the thiophene ring allows for further functionalization, making it versatile in designing molecules with specific properties. Additionally, it finds application in material science for synthesizing conjugated polymers and organic electronic materials, which are essential in the production of organic light-emitting diodes (OLEDs) and other advanced materials. Its boronic acid moiety enables efficient cross-coupling with aryl halides, facilitating the construction of carbon-carbon bonds in a controlled manner.
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