2-Methoxypyridine-5-boronic acid pinacol ester

97%

Reagent Code: #89853
label
Alias 2-Methoxypyridine-5-boronic acid pinacol ester 2-Methoxy-5-pyridineboronic acid pinacol ester 2-Methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
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CAS Number 445264-61-9

science Other reagents with same CAS 445264-61-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 235.09 g/mol
Formula C₁₂H₁₈BNO₃
badge Registry Numbers
MDL Number MFCD05663858
thermostat Physical Properties
Melting Point 47-51 °C(lit.)
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key intermediate for forming carbon-carbon bonds. Its boronic ester group enables efficient coupling with aryl or vinyl halides, facilitating the creation of complex organic molecules. It is commonly employed in pharmaceutical research and development for constructing drug candidates, especially in the synthesis of heterocyclic compounds. Additionally, it finds use in material science for designing advanced polymers and organic electronic materials. Its stability and reactivity make it a valuable reagent in catalytic processes and fine chemical production.

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Test Parameter Specification
Purity (HPLC) 97-100%
Appearance White to yellow solid
Infrared Spectrum Conforms to Structure
Proton NMR Spectrum Conforms to Structure
Note Low melting point solid; may change state in different environments (solid, liquid, or semi-solid)

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿290.00
inventory 1g
10-20 days ฿430.00
inventory 5g
10-20 days ฿1,610.00

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2-Methoxypyridine-5-boronic acid pinacol ester
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This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key intermediate for forming carbon-carbon bonds. Its boronic ester group enables efficient coupling with aryl or vinyl halides, facilitating the creation of complex organic molecules. It is commonly employed in pharmaceutical research and development for constructing drug candidates, especially in the synthesis of heterocyclic compounds. Additionally, it finds use in material science for designing advanced polymers and organic electronic materials. Its stability and reactivity make it a valuable reagent in catalytic processes and fine chemical production.
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