2-(((tert-Butyldimethylsilyl)oxy)methyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

98%

Reagent Code: #153633
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CAS Number 880495-84-1

science Other reagents with same CAS 880495-84-1

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inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its pyridine core with a boronate ester group allows for selective coupling with aryl or heteroaryl halides, making it valuable in constructing complex nitrogen-containing molecules. The silyl-protected hydroxymethyl group offers a handle for further functionalization, commonly used in multistep organic synthesis, particularly in drug discovery and development of bioactive compounds.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,190.00
inventory 250mg
10-20 days ฿4,330.00

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2-(((tert-Butyldimethylsilyl)oxy)methyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its pyridine core with a boronate ester group allows for selective coupling with aryl or heteroaryl halides, making it valuable in constructing complex nitrogen-containing molecules. The silyl-protected hydroxymethyl group offers a handle for further functionalization, commonly used in multistep organic synthesis, particularly in drug discovery

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its pyridine core with a boronate ester group allows for selective coupling with aryl or heteroaryl halides, making it valuable in constructing complex nitrogen-containing molecules. The silyl-protected hydroxymethyl group offers a handle for further functionalization, commonly used in multistep organic synthesis, particularly in drug discovery and development of bioactive compounds.

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