3-Isopropoxybenzeneboronic acid

97%

Reagent Code: #90135
label
Alias 3-Isopropoxyphenylboronic acid
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CAS Number 216485-86-8

science Other reagents with same CAS 216485-86-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 180.01 g/mol
Formula C₉H₁₃BO₃
badge Registry Numbers
MDL Number MFCD03701512
thermostat Physical Properties
Melting Point 76-81 °C(lit.)
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a crucial building block for creating complex organic molecules, often used in the pharmaceutical industry to develop drug candidates. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of biaryl structures, which are common in many active pharmaceutical ingredients. Additionally, it finds applications in material science, where it aids in the synthesis of organic electronic materials and polymers. Its stability and reactivity make it a valuable reagent in research and industrial processes.

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Test Parameter Specification
Purity (Titration by NaOH) 97-100%
Appearance White to grey powder or crystals
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 ฿1,580.00
inventory 25g
10-20 days ฿6,620.00
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3-Isopropoxybenzeneboronic acid
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This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a crucial building block for creating complex organic molecules, often used in the pharmaceutical industry to develop drug candidates. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of biaryl structures, which are common in many active pharmaceutical ingredients. Additionally, it finds applications in material science, where it aids in the synthesis of organic electronic materials and polymers. Its stability and reactivity make it a valuable reagent in research and industrial processes.
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