3-Pyridineboronic acid pinacol ester

98%

Reagent Code: #90129
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CAS Number 329214-79-1

science Other reagents with same CAS 329214-79-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 205.06 g/mol
Formula C₁₁H₁₆BNO₂
badge Registry Numbers
MDL Number MFCD03084758
thermostat Physical Properties
Melting Point 102-104.4 °C(lit.)
inventory_2 Storage & Handling
Density 1.03g/cm3
Storage 2~8℃

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, facilitating the synthesis of biaryl compounds widely applied in pharmaceuticals and agrochemicals. Its boronic ester group enables efficient coupling with aryl halides, making it valuable in creating complex organic molecules. Commonly employed in the development of drugs targeting various diseases, including cancer and inflammation. Also utilized in material science for constructing organic electronic materials and polymers. Its stability and reactivity make it a preferred choice in organic synthesis and industrial applications.

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Test Parameter Specification
Purity 97.5-100%
Appearance White to tan powder or crystals
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿300.00
inventory 25g
10-20 days ฿2,890.00
inventory 5g
10-20 days ฿910.00
inventory 100g
10-20 days ฿10,680.00

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3-Pyridineboronic acid pinacol ester
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, facilitating the synthesis of biaryl compounds widely applied in pharmaceuticals and agrochemicals. Its boronic ester group enables efficient coupling with aryl halides, making it valuable in creating complex organic molecules. Commonly employed in the development of drugs targeting various diseases, including cancer and inflammation. Also utilized in material science for constructing organic electronic materials and polymers. Its sta

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, facilitating the synthesis of biaryl compounds widely applied in pharmaceuticals and agrochemicals. Its boronic ester group enables efficient coupling with aryl halides, making it valuable in creating complex organic molecules. Commonly employed in the development of drugs targeting various diseases, including cancer and inflammation. Also utilized in material science for constructing organic electronic materials and polymers. Its stability and reactivity make it a preferred choice in organic synthesis and industrial applications.

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