4-Carboxy-3-fluorophenylboronic acid

98%

Reagent Code: #90722
label
Alias 4-Carboxy-3-fluorophenylboronic acid 3-fluoro-4-carboxyphenylboronic acid
fingerprint
CAS Number 120153-08-4

science Other reagents with same CAS 120153-08-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 183.93 g/mol
Formula C₇H₆BFO₄
badge Registry Numbers
MDL Number MFCD01114671
thermostat Physical Properties
Melting Point 236-240°C
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

This chemical is primarily used as a building block in organic synthesis, particularly in the preparation of pharmaceuticals and biologically active compounds. It is often employed in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds, due to the presence of the boronic acid group. The fluorine substituent can enhance the stability and reactivity of the molecule, making it valuable in the development of drug candidates or materials with specific properties. Additionally, its carboxylic acid group allows for further functionalization, enabling its use in creating complex molecular structures. This compound is also explored in research for potential applications in medicinal chemistry, such as enzyme inhibitors or receptor-targeting molecules.

format_list_bulleted Product Specification

Test Parameter Specification
Melting point 236-240
Purity (HPLC) 98-100%
Appearance White to off-white solid
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿470.00
inventory 5g
10-20 days ฿1,980.00
inventory 25g
10-20 days ฿9,100.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
4-Carboxy-3-fluorophenylboronic acid
No image available
This chemical is primarily used as a building block in organic synthesis, particularly in the preparation of pharmaceuticals and biologically active compounds. It is often employed in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds, due to the presence of the boronic acid group. The fluorine substituent can enhance the stability and reactivity of the molecule, making it valuable in the development of drug candidates or materials with specific properties. Additionally, its carboxylic acid group allows for further functionalization, enabling its use in creating complex molecular structures. This compound is also explored in research for potential applications in medicinal chemistry, such as enzyme inhibitors or receptor-targeting molecules.
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...