Pyridine-2-boronic acid

95%

Reagent Code: #91120
label
Alias 2-Pyridineboronic acid
fingerprint
CAS Number 197958-29-5

science Other reagents with same CAS 197958-29-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 122.92 g/mol
Formula C₅H₆BNO₂
badge Registry Numbers
MDL Number MFCD00151844
thermostat Physical Properties
Melting Point >300
inventory_2 Storage & Handling
Storage -20°C

description Product Description

Pyridine-2-boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for forming carbon-carbon bonds, enabling the synthesis of complex biaryl compounds. This chemical is also utilized in the preparation of pharmaceuticals and agrochemicals, where it acts as a building block for creating active ingredients. Additionally, it finds application in material science for developing organic electronic materials and polymers. Its boronic acid group allows for selective binding with diols, making it useful in sensor development and carbohydrate recognition studies.

format_list_bulleted Product Specification

Test Parameter Specification
Purity 95-100%
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿990.00
inventory 1g
10-20 days ฿3,120.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Pyridine-2-boronic acid
No image available

Pyridine-2-boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for forming carbon-carbon bonds, enabling the synthesis of complex biaryl compounds. This chemical is also utilized in the preparation of pharmaceuticals and agrochemicals, where it acts as a building block for creating active ingredients. Additionally, it finds application in material science for developing organic electronic materials and polymers. Its boronic

Pyridine-2-boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for forming carbon-carbon bonds, enabling the synthesis of complex biaryl compounds. This chemical is also utilized in the preparation of pharmaceuticals and agrochemicals, where it acts as a building block for creating active ingredients. Additionally, it finds application in material science for developing organic electronic materials and polymers. Its boronic acid group allows for selective binding with diols, making it useful in sensor development and carbohydrate recognition studies.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...