4-Chlorophenylboronic acid

97%

Reagent Code: #90647
label
Alias 4-Chlorophenylboronic acid; p-chlorophenylboronic acid
fingerprint
CAS Number 1679-18-1

science Other reagents with same CAS 1679-18-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 156.37 g/mol
Formula C₆H₆BClO₂
badge Registry Numbers
EC Number 216-845-5
MDL Number MFCD00039137
thermostat Physical Properties
Melting Point 284-289 °C(lit.)
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

4-Chlorophenylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the creation of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its role as a boronic acid derivative makes it a valuable reagent for constructing biaryl compounds, which are common in drug development. Additionally, it serves as a building block in the synthesis of sensors and catalysts, contributing to advancements in chemical detection and industrial processes. Its stability and reactivity make it a preferred choice in various research and industrial applications.

format_list_bulleted Product Specification

Test Parameter Specification
Purity 97-100
Appearance White to tan crystal or powder
Infrared Spectrum Conforms to Structure
1H NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿310.00
inventory 5g
10-20 days ฿420.00
inventory 25g
10-20 days ฿980.00
inventory 100g
10-20 days ฿2,900.00
inventory 500g
10-20 days ฿13,860.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
4-Chlorophenylboronic acid
No image available

4-Chlorophenylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the creation of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its role as a boronic acid derivative makes it a valuable reagent for constructing biaryl compounds, which are common in drug development. Additionally, it serves as a building block in the synthesis of sensors

4-Chlorophenylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the creation of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its role as a boronic acid derivative makes it a valuable reagent for constructing biaryl compounds, which are common in drug development. Additionally, it serves as a building block in the synthesis of sensors and catalysts, contributing to advancements in chemical detection and industrial processes. Its stability and reactivity make it a preferred choice in various research and industrial 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...