4-Acetoxyphenylboronic acid pinacol ester

97%

Reagent Code: #90552
label
Alias 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl acetate
fingerprint
CAS Number 480424-70-2

science Other reagents with same CAS 480424-70-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 262.11 g/mol
Formula C₆H₄OCOCH₃BO₂C₂CH₃₄
badge Registry Numbers
MDL Number MFCD03453060
thermostat Physical Properties
Melting Point 67-71 °C(lit.)
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Used in organic synthesis as a key intermediate for the preparation of various bioactive molecules and pharmaceuticals. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic compounds. This chemical is also employed in the development of sensors and probes for detecting specific analytes due to its boronic acid functionality, which can selectively bind to diols and sugars. Additionally, it finds application in material science for the modification of surfaces and the creation of functionalized polymers.

format_list_bulleted Product Specification

Test Parameter Specification
Melting point 67-71
Purity (HPLC) 97-100
Appearance White to off-white powder
Infrared Spectrometry Conforms to Structure
Proton NMR Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿1,350.00
inventory 1g
10-20 days ฿2,230.00
inventory 5g
10-20 days ฿8,900.00
inventory 25g
10-20 days ฿39,880.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
4-Acetoxyphenylboronic acid pinacol ester
No image available
Used in organic synthesis as a key intermediate for the preparation of various bioactive molecules and pharmaceuticals. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic compounds. This chemical is also employed in the development of sensors and probes for detecting specific analytes due to its boronic acid functionality, which can selectively bind to diols and sugars. Additionally, it finds application in material scienc
Used in organic synthesis as a key intermediate for the preparation of various bioactive molecules and pharmaceuticals. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic compounds. This chemical is also employed in the development of sensors and probes for detecting specific analytes due to its boronic acid functionality, which can selectively bind to diols and sugars. Additionally, it finds application in material science for the modification of surfaces and the creation of functionalized polymers.
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...