4-Formylphenylboronic acid

>98%

Reagent Code: #90707
label
Alias 4-Formylphenylboronic acid; p-formylphenylboronic acid, p-formylphenylboronic acid
fingerprint
CAS Number 87199-17-5

science Other reagents with same CAS 87199-17-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 149.94 g/mol
Formula C₇H₇BO₃
badge Registry Numbers
MDL Number MFCD00151823
thermostat Physical Properties
Melting Point 237-242 °C(lit.)
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, it facilitates the formation of carbon-carbon bonds, essential in synthesizing complex organic molecules. It is also employed in the development of sensors for detecting sugars and other diol-containing compounds due to its ability to form reversible covalent bonds with 1,2- or 1,3-diols. Additionally, it serves as a building block in the preparation of pharmaceutical intermediates and materials for organic electronics. Its aldehyde group allows for further functionalization, making it versatile in organic synthesis and material science.

format_list_bulleted Product Specification

Test Parameter Specification
Purity (HPLC) 97-100
Appearance White to off-white to yellow powder
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿1,960.00
inventory 1g
10-20 days ฿320.00
inventory 5g
10-20 days ฿660.00
inventory 100g
10-20 days ฿6,220.00

Cart

No products

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

Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, it facilitates the formation of carbon-carbon bonds, essential in synthesizing complex organic molecules. It is also employed in the development of sensors for detecting sugars and other diol-containing compounds due to its ability to form reversible covalent bonds with 1,2- or 1,3-diols. Additionally, it serves as a building block in the preparation of pharmaceutical intermediates and materials for organic electronics. Its aldehyde group

Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, it facilitates the formation of carbon-carbon bonds, essential in synthesizing complex organic molecules. It is also employed in the development of sensors for detecting sugars and other diol-containing compounds due to its ability to form reversible covalent bonds with 1,2- or 1,3-diols. Additionally, it serves as a building block in the preparation of pharmaceutical intermediates and materials for organic electronics. Its aldehyde group allows for further functionalization, making it versatile in organic synthesis and material science.

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...