3-Chloro-4-fluorophenylboronic acid

98%

Reagent Code: #90209
label
Alias 3-Chloro-4-fluorophenylboronic acid
fingerprint
CAS Number 144432-85-9

science Other reagents with same CAS 144432-85-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 174.37 g/mol
Formula C₆H₅BClFO₂
badge Registry Numbers
MDL Number MFCD00051800
thermostat Physical Properties
Melting Point 242-247 °C(lit.)
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

Widely used in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate in the synthesis of complex organic molecules, particularly in pharmaceuticals and agrochemicals. Its boronic acid group enables efficient coupling with aryl halides, facilitating the creation of biaryl structures essential in drug development. Additionally, it is employed in the production of liquid crystals and organic electronic materials, where precise molecular architecture is critical. The chloro and fluoro substituents enhance its reactivity and selectivity, making it valuable in fine chemical synthesis and material science applications.

format_list_bulleted Product Specification

Test Parameter Specification
Purity 98-100
Appearance White to off-white powder
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿290.00
inventory 5g
10-20 days ฿970.00
inventory 25g
10-20 days ฿3,860.00
inventory 100g
10-20 days ฿12,800.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
3-Chloro-4-fluorophenylboronic acid
No image available

Widely used in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate in the synthesis of complex organic molecules, particularly in pharmaceuticals and agrochemicals. Its boronic acid group enables efficient coupling with aryl halides, facilitating the creation of biaryl structures essential in drug development. Additionally, it is employed in the production of liquid crystals and organic electronic materials, where precise molecular architecture is critical. The chloro and

Widely used in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate in the synthesis of complex organic molecules, particularly in pharmaceuticals and agrochemicals. Its boronic acid group enables efficient coupling with aryl halides, facilitating the creation of biaryl structures essential in drug development. Additionally, it is employed in the production of liquid crystals and organic electronic materials, where precise molecular architecture is critical. The chloro and fluoro substituents enhance its reactivity and selectivity, making it valuable in fine chemical synthesis and material science applications.

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...