3-(Hydroxymethyl)phenylboronic acid

>98%

Reagent Code: #90270
label
Alias 3-Hydroxymethylphenylboronic acid
fingerprint
CAS Number 87199-15-3

science Other reagents with same CAS 87199-15-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 151.96 g/mol
Formula C₇H₉BO₃
badge Registry Numbers
MDL Number MFCD01317846
thermostat Physical Properties
Melting Point 95-99 °C(lit.)
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key reagent for forming carbon-carbon bonds. It is also employed in the development of sensors and diagnostic tools due to its ability to bind with diols and sugars, making it useful in glucose detection systems. Additionally, it finds applications in the preparation of pharmaceutical intermediates and in materials science for creating functionalized polymers and coatings. Its boronic acid group enables it to serve as a versatile building block in various chemical and biochemical research applications.

format_list_bulleted Product Specification

Test Parameter Specification
Purity (HPLC) 98-100%
Melting Point (°C) 95-99

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿580.00
inventory 1g
10-20 days ฿320.00
inventory 25g
10-20 days ฿2,680.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
3-(Hydroxymethyl)phenylboronic acid
No image available

This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key reagent for forming carbon-carbon bonds. It is also employed in the development of sensors and diagnostic tools due to its ability to bind with diols and sugars, making it useful in glucose detection systems. Additionally, it finds applications in the preparation of pharmaceutical intermediates and in materials science for creating functionalized polymers and coatings. Its bo

This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key reagent for forming carbon-carbon bonds. It is also employed in the development of sensors and diagnostic tools due to its ability to bind with diols and sugars, making it useful in glucose detection systems. Additionally, it finds applications in the preparation of pharmaceutical intermediates and in materials science for creating functionalized polymers and coatings. Its boronic acid group enables it to serve as a versatile building block in various chemical and biochemical research 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...