3,5-Dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

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Reagent Code: #178056
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CAS Number 1257641-28-3

science Other reagents with same CAS 1257641-28-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 273.95 g/mol
Formula C₁₁H₁₄BCl₂NO₂
badge Registry Numbers
MDL Number MFCD12546037
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used primarily in cross-coupling reactions, this compound serves as a key building block in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient Suzuki-Miyaura coupling, allowing the formation of carbon-carbon bonds with aryl or heteroaryl halides under palladium catalysis. It is especially valuable in medicinal chemistry for constructing complex pyridine-based scaffolds found in bioactive molecules. The presence of chlorine atoms offers additional sites for selective functionalization, enabling further structural diversification in drug discovery and materials science.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,070.00
inventory 250mg
10-20 days ฿1,950.00
inventory 1g
10-20 days ฿5,510.00

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3,5-Dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
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Used primarily in cross-coupling reactions, this compound serves as a key building block in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient Suzuki-Miyaura coupling, allowing the formation of carbon-carbon bonds with aryl or heteroaryl halides under palladium catalysis. It is especially valuable in medicinal chemistry for constructing complex pyridine-based scaffolds found in bioactive molecules. The presence of chlorine atoms offers additional sites for sele

Used primarily in cross-coupling reactions, this compound serves as a key building block in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient Suzuki-Miyaura coupling, allowing the formation of carbon-carbon bonds with aryl or heteroaryl halides under palladium catalysis. It is especially valuable in medicinal chemistry for constructing complex pyridine-based scaffolds found in bioactive molecules. The presence of chlorine atoms offers additional sites for selective functionalization, enabling further structural diversification in drug discovery and materials science.

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