(2-Ethylpyridin-3-yl)boronic acid

≥95%

Reagent Code: #113072
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CAS Number 1310384-02-1

science Other reagents with same CAS 1310384-02-1

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Weight 150.97 g/mol
Formula C₇H₁₀BNO₂
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MDL Number MFCD07374992
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

(2-Ethylpyridin-3-yl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound acts as a key intermediate in the synthesis of complex molecules, including drug candidates and bioactive compounds. Its boronic acid group facilitates efficient coupling with aryl or vinyl halides, enabling the creation of diverse chemical structures. Additionally, it is employed in the development of sensors and catalysts due to its ability to interact with various organic and inorganic substrates.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿8,829.00

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(2-Ethylpyridin-3-yl)boronic acid
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(2-Ethylpyridin-3-yl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound acts as a key intermediate in the synthesis of complex molecules, including drug candidates and bioactive compounds. Its boronic acid group facilitates efficient coupling with aryl or vinyl halides, enabling the

(2-Ethylpyridin-3-yl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound acts as a key intermediate in the synthesis of complex molecules, including drug candidates and bioactive compounds. Its boronic acid group facilitates efficient coupling with aryl or vinyl halides, enabling the creation of diverse chemical structures. Additionally, it is employed in the development of sensors and catalysts due to its ability to interact with various organic and inorganic substrates.

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