3-Methoxycarbonylphenylboronic acid

97%

Reagent Code: #90250
label
Alias 3-Methoxycarbonylphenylboronic acid
fingerprint
CAS Number 99769-19-4

science Other reagents with same CAS 99769-19-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 179.97 g/mol
Formula C₈H₉BO₄
badge Registry Numbers
MDL Number MFCD02093046
thermostat Physical Properties
Melting Point 205-208 °C(lit.)
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of pharmaceuticals and agrochemicals. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, where it facilitates the formation of carbon-carbon bonds, enabling the synthesis of complex organic molecules. Additionally, it finds application in the development of sensors and diagnostic agents due to its boronic acid group, which can selectively bind to diols and sugars. This property is exploited in glucose sensing technologies and other biochemical assays. Its versatility also extends to materials science, where it is used in the modification of polymers and the creation of advanced materials with specific functionalities.

format_list_bulleted Product Specification

Test Parameter Specification
Purity (HPLC) 97-100%
Purity (Neutralization Titration) 96.5-103.5%
Appearance White to light yellow powder
Infrared Spectrum Conforms to Structure
Proton NMR Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿400.00
inventory 5g
10-20 days ฿1,280.00
inventory 25g
10-20 days ฿4,400.00
inventory 100g
10-20 days ฿15,370.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
3-Methoxycarbonylphenylboronic acid
No image available

Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of pharmaceuticals and agrochemicals. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, where it facilitates the formation of carbon-carbon bonds, enabling the synthesis of complex organic molecules. Additionally, it finds application in the development of sensors and diagnostic agents due to its boronic acid group, which can selectively bind to diols and sugars. This property is explo

Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of pharmaceuticals and agrochemicals. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, where it facilitates the formation of carbon-carbon bonds, enabling the synthesis of complex organic molecules. Additionally, it finds application in the development of sensors and diagnostic agents due to its boronic acid group, which can selectively bind to diols and sugars. This property is exploited in glucose sensing technologies and other biochemical assays. Its versatility also extends to materials science, where it is used in the modification of polymers and the creation of advanced materials with specific functionalities.

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...