(2-(thiophen-2-yl)pyrimidin-5-yl)boronic acid

95%

Reagent Code: #56364
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CAS Number 2225172-17-6

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 206.02938 g/mol
Formula C₈H₇BN₂O₂S
inventory_2 Storage & Handling
Storage -20℃, sealed and dry

description Product Description

This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for the formation of carbon-carbon bonds, enabling the creation of complex organic molecules. Its boronic acid group reacts efficiently with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its thiophene and pyrimidine moieties contribute to its utility in designing compounds with potential biological activity, such as drug candidates targeting various diseases. Its role in material science is also notable, as it aids in the development of organic electronic components like OLEDs and semiconductors.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5mg
10-20 days ฿14,260.00
25mg
10-20 days ฿49,200.00
100mg
10-20 days ฿127,400.00
(2-(thiophen-2-yl)pyrimidin-5-yl)boronic acid
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This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for the formation of carbon-carbon bonds, enabling the creation of complex organic molecules. Its boronic acid group reacts efficiently with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its thiophene and pyrimidine moieties contribute to i

This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for the formation of carbon-carbon bonds, enabling the creation of complex organic molecules. Its boronic acid group reacts efficiently with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its thiophene and pyrimidine moieties contribute to its utility in designing compounds with potential biological activity, such as drug candidates targeting various diseases. Its role in material science is also notable, as it aids in the development of organic electronic components like OLEDs and semiconductors.

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