(E)-3-(2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)vinyl)pyridine

97%

Reagent Code: #181103
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CAS Number 950483-20-2

science Other reagents with same CAS 950483-20-2

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Weight 231.1 g/mol
Formula C₁₃H₁₈BNO₂
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MDL Number MFCD06659958
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of conjugated organic materials. It is particularly valuable in the development of organic semiconductors, OLEDs (organic light-emitting diodes), and pharmaceuticals due to its ability to introduce pyridine-based vinyl structures into larger π-conjugated systems. The boronate ester group enables efficient and selective bond formation with aryl or vinyl halides under mild palladium catalysis. Its (E)-configuration ensures structural rigidity and optimal electronic properties in the final products. Commonly employed in research and industrial settings for fabricating advanced functional materials.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,120.00
inventory 1g
10-20 days ฿18,160.00
inventory 5g
10-20 days ฿63,530.00

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(E)-3-(2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)vinyl)pyridine
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of conjugated organic materials. It is particularly valuable in the development of organic semiconductors, OLEDs (organic light-emitting diodes), and pharmaceuticals due to its ability to introduce pyridine-based vinyl structures into larger π-conjugated systems. The boronate ester group enables efficient and selective bond formation with aryl or vinyl halides under mild palladium catalysis. Its (E)-configuration ensu

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of conjugated organic materials. It is particularly valuable in the development of organic semiconductors, OLEDs (organic light-emitting diodes), and pharmaceuticals due to its ability to introduce pyridine-based vinyl structures into larger π-conjugated systems. The boronate ester group enables efficient and selective bond formation with aryl or vinyl halides under mild palladium catalysis. Its (E)-configuration ensures structural rigidity and optimal electronic properties in the final products. Commonly employed in research and industrial settings for fabricating advanced functional materials.

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