Dibenzo[b,d]Furan-3-Ylboronic Acid

99%

Reagent Code: #91096
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CAS Number 395087-89-5

science Other reagents with same CAS 395087-89-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 212.01 g/mol
Formula C₁₂H₉BO₃
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for creating complex organic molecules, especially in the pharmaceutical industry, where it helps in the development of drug candidates. Its boronic acid group enables efficient coupling with aryl halides, making it valuable for constructing biaryl structures, which are common in many active pharmaceutical ingredients. Additionally, it is utilized in material science for synthesizing organic semiconductors and polymers, contributing to advancements in electronic devices and optoelectronic materials. Its stability and reactivity make it a preferred choice in various research and industrial applications.

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Test Parameter Specification
Appearance Off-White Powder
Purity 98.5-100
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿4,840.00
inventory 1g
10-20 days ฿1,900.00
inventory 25g
10-20 days ฿16,670.00

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Dibenzo[b,d]Furan-3-Ylboronic Acid
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This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for creating complex organic molecules, especially in the pharmaceutical industry, where it helps in the development of drug candidates. Its boronic acid group enables efficient coupling with aryl halides, making it valuable for constructing biaryl structures, which are common in many active pharmaceutical ingredients. Additionally, it is utilized in material scien

This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for creating complex organic molecules, especially in the pharmaceutical industry, where it helps in the development of drug candidates. Its boronic acid group enables efficient coupling with aryl halides, making it valuable for constructing biaryl structures, which are common in many active pharmaceutical ingredients. Additionally, it is utilized in material science for synthesizing organic semiconductors and polymers, contributing to advancements in electronic devices and optoelectronic materials. Its stability and reactivity make it a preferred choice in various research and industrial applications.

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