4'-Borono-[1,1'-Biphenyl]-4-Carboxylic Acid

≥98%

Reagent Code: #90291
fingerprint
CAS Number 872341-95-2

science Other reagents with same CAS 872341-95-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 242.04 g/mol
Formula C₁₃H₁₁BO₄
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key reagent for forming carbon-carbon bonds. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is used in the development of boron-based drugs and as a building block in the synthesis of complex organic molecules. Its applications extend to material science, where it contributes to the creation of organic electronic components and polymers.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White like powder
Purity (%) 98-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿2,052.00
inventory 1g
10-20 days ฿8,235.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
4'-Borono-[1,1'-Biphenyl]-4-Carboxylic Acid
No image available

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key reagent for forming carbon-carbon bonds. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is used in the development of boron-based drugs and as a building block in the synthesis of complex organic molecules. Its applications extend to

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key reagent for forming carbon-carbon bonds. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is used in the development of boron-based drugs and as a building block in the synthesis of complex organic molecules. Its applications extend to material science, where it contributes to the creation of organic electronic components and polymers.

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...