3-Methylpyridine-2-boronic acid

95%

Reagent Code: #208810
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CAS Number 930303-26-7

science Other reagents with same CAS 930303-26-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 136.94 g/mol
Formula C₆H₈BNO₂
badge Registry Numbers
MDL Number MFCD00674178
thermostat Physical Properties
Boiling Point 323.9°C at 760 mmHg
inventory_2 Storage & Handling
Storage -20°C, dry seal

description Product Description

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to construct carbon-carbon bonds. It serves as a key building block in the development of pharmaceuticals and agrochemicals, where the pyridine ring system is a common structural motif. Its boronic acid group enables efficient coupling with aryl or vinyl halides under palladium catalysis, making it valuable in medicinal chemistry for creating complex heterocyclic compounds. Also applied in materials science for designing functional organic molecules with electronic properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,310.00
inventory 1g
10-20 days ฿21,100.00
inventory 250mg
10-20 days ฿8,440.00

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3-Methylpyridine-2-boronic acid
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Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to construct carbon-carbon bonds. It serves as a key building block in the development of pharmaceuticals and agrochemicals, where the pyridine ring system is a common structural motif. Its boronic acid group enables efficient coupling with aryl or vinyl halides under palladium catalysis, making it valuable in medicinal chemistry for creating complex heterocyclic compounds. Also applied in materials science for designing f

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to construct carbon-carbon bonds. It serves as a key building block in the development of pharmaceuticals and agrochemicals, where the pyridine ring system is a common structural motif. Its boronic acid group enables efficient coupling with aryl or vinyl halides under palladium catalysis, making it valuable in medicinal chemistry for creating complex heterocyclic compounds. Also applied in materials science for designing functional organic molecules with electronic properties.

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