4-Cyano-3-fluorobenzeneboronic acid

97%

Reagent Code: #90648
label
Alias 4-cyano-3-fluorophenylboronic acid
fingerprint
CAS Number 843663-18-3

science Other reagents with same CAS 843663-18-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 164.94 g/mol
Formula C₇H₅BFNO₂
badge Registry Numbers
MDL Number MFCD03411549
thermostat Physical Properties
Melting Point 362-366
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key building block for creating complex organic molecules. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in pharmaceutical research for developing drug candidates. Additionally, the presence of both cyano and fluoro groups enhances its reactivity and selectivity, allowing for the synthesis of diverse aromatic compounds. It is also employed in material science for designing advanced polymers and electronic materials, where its structural properties contribute to improved performance and stability.

format_list_bulleted Product Specification

Test Parameter Specification
Melting point 362-366
Purity (GC) 97-100
Appearance White to light yellow powder
Infrared Spectrometry Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿2,200.00
inventory 1g
10-20 days ฿580.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
4-Cyano-3-fluorobenzeneboronic acid
No image available

This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key building block for creating complex organic molecules. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in pharmaceutical research for developing drug candidates. Additionally, the presence of both cyano and fluoro groups enhances its reactivity and selectivity, allowing for the synthesis of diverse aromatic compounds. It is also emplo

This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key building block for creating complex organic molecules. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in pharmaceutical research for developing drug candidates. Additionally, the presence of both cyano and fluoro groups enhances its reactivity and selectivity, allowing for the synthesis of diverse aromatic compounds. It is also employed in material science for designing advanced polymers and electronic materials, where its structural properties contribute to improved performance and stability.

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...