3-Chloro-4-methoxyphenylboronic acid

98%

Reagent Code: #90212
label
Alias 3-Chloro-4-methoxyphenylboronic acid
fingerprint
CAS Number 175883-60-0

science Other reagents with same CAS 175883-60-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 186.4 g/mol
Formula ClC₆H₃OCH₃BOH₂
badge Registry Numbers
MDL Number MFCD04039888
thermostat Physical Properties
Melting Point 238-242 °C(lit.)
inventory_2 Storage & Handling
Density 1.32
Storage 2~8°C

description Product Description

This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for creating complex organic molecules, often in pharmaceutical research and development. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable for constructing biologically active compounds. Additionally, it is utilized in the production of materials for organic electronics, such as OLEDs, due to its ability to modify conjugated systems. Its applications also extend to the development of sensors and catalysts, where its structural properties enhance performance and specificity.

format_list_bulleted Product Specification

Test Parameter Specification
Purity (HPLC) 98-100
Melting point 238-242
Appearance White to off-white powder
Infrared Spectrum Conforms to Structure
Proton NMR Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿8,180.00
inventory 1g
10-20 days ฿700.00
inventory 5g
10-20 days ฿2,320.00

Cart

No products

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

This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for creating complex organic molecules, often in pharmaceutical research and development. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable for constructing biologically active compounds. Additionally, it is utilized in the production of materials for organic electronics, such as OLEDs, due to its ability to modify conjugate

This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for creating complex organic molecules, often in pharmaceutical research and development. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable for constructing biologically active compounds. Additionally, it is utilized in the production of materials for organic electronics, such as OLEDs, due to its ability to modify conjugated systems. Its applications also extend to the development of sensors and catalysts, where its structural properties enhance performance and specificity.

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...