4-Chloro-2-(trifluoromethyl)benzeneboronic acid

98%

Reagent Code: #90623
label
Alias 4-Chloro-2-(trifluoromethyl)phenylboronic acid 2-trifluoromethyl-4-4chloroboronic acid
fingerprint
CAS Number 313545-41-4

science Other reagents with same CAS 313545-41-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 224.38 g/mol
Formula C₇H₅BClF₃O₂
badge Registry Numbers
MDL Number MFCD08274479
thermostat Physical Properties
Melting Point 70-72
inventory_2 Storage & Handling
Storage 2~8℃

description Product Description

This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for creating complex organic molecules, including pharmaceuticals and agrochemicals. Its boronic acid group enables efficient coupling with aryl halides, making it valuable for constructing biaryl compounds. Additionally, it is utilized in the development of advanced materials, such as liquid crystals and polymers, due to its ability to introduce trifluoromethyl groups, which enhance stability and performance. Its applications also extend to research in medicinal chemistry, where it aids in the synthesis of potential drug candidates.

format_list_bulleted Product Specification

Test Parameter Specification
Purity (Neutralization Titration) 97-100
Appearance White to off-white powder or crystals
Infrared Spectrometry Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿330.00
inventory 5g
10-20 days ฿1,510.00
inventory 25g
10-20 days ฿6,920.00
inventory 100g
10-20 days ฿27,130.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
4-Chloro-2-(trifluoromethyl)benzeneboronic acid
No image available
This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for creating complex organic molecules, including pharmaceuticals and agrochemicals. Its boronic acid group enables efficient coupling with aryl halides, making it valuable for constructing biaryl compounds. Additionally, it is utilized in the development of advanced materials, such as liquid crystals and polymers, due to its ability to introduce trifluoromethyl groups, which enhance stability and performance. Its applications also extend to research in medicinal chemistry, where it aids in the synthesis of potential drug candidates.
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...