2-Chloropyridine-4-boronic acid pinacol ester

98%

Reagent Code: #89798
label
Alias 2-Chloro-pyridine-4-boronic acid pinacol ester 2-Chloro-4-pyridineboronic acid pinacol ester
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CAS Number 458532-84-8

science Other reagents with same CAS 458532-84-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 239.51 g/mol
Formula C₁₁H₁₅BClNO₂
badge Registry Numbers
MDL Number MFCD04039870
thermostat Physical Properties
Melting Point 64.7-64.8°C
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Used extensively in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate in the synthesis of complex organic molecules, particularly in pharmaceutical research. Its boronic ester group facilitates the formation of carbon-carbon bonds, enabling the creation of diverse pyridine derivatives. These derivatives are crucial in developing active pharmaceutical ingredients (APIs) and agrochemicals. Additionally, it is employed in material science for designing advanced polymers and functional materials. Its stability and reactivity make it a valuable tool in organic synthesis and drug discovery pipelines.

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Test Parameter Specification
Purity (HPLC) 98-100
Infrared Spectrometry Conforms to Structure
Proton NMR Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,310.00
inventory 5g
10-20 days ฿5,080.00

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2-Chloropyridine-4-boronic acid pinacol ester
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Used extensively in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate in the synthesis of complex organic molecules, particularly in pharmaceutical research. Its boronic ester group facilitates the formation of carbon-carbon bonds, enabling the creation of diverse pyridine derivatives. These derivatives are crucial in developing active pharmaceutical ingredients (APIs) and agrochemicals. Additionally, it is employed in material science for designing advanced polymers and

Used extensively in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate in the synthesis of complex organic molecules, particularly in pharmaceutical research. Its boronic ester group facilitates the formation of carbon-carbon bonds, enabling the creation of diverse pyridine derivatives. These derivatives are crucial in developing active pharmaceutical ingredients (APIs) and agrochemicals. Additionally, it is employed in material science for designing advanced polymers and functional materials. Its stability and reactivity make it a valuable tool in organic synthesis and drug discovery pipelines.

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