Dibenzo[b,d]furan-1-ylboronicacid

99%

Reagent Code: #91095
label
Alias 1-Dibenzofurylboronic acid
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CAS Number 162607-19-4

science Other reagents with same CAS 162607-19-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 212.01 g/mol
Formula C₁₂H₉BO₃
badge Registry Numbers
MDL Number MFCD01318978
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key reagent for constructing complex organic molecules, especially in the pharmaceutical and materials science industries. Its boronic acid functional group enables the formation of carbon-carbon bonds, making it valuable for creating aryl-aryl linkages in drug development and advanced materials. Additionally, it is employed in the synthesis of organic electronic materials, including polymers and small molecules used in OLEDs and other optoelectronic devices. Its ability to introduce aromatic structures into compounds makes it a versatile tool in designing molecules with specific electronic or photophysical properties.

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Test Parameter Specification
Appearance White to Almost White Powder to Crystal
Purity (%) 98.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿522.00
inventory 1g
10-20 days ฿2,115.00
inventory 5g
10-20 days ฿7,443.00
inventory 25g
10-20 days ฿33,507.00

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Dibenzo[b,d]furan-1-ylboronicacid
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This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key reagent for constructing complex organic molecules, especially in the pharmaceutical and materials science industries. Its boronic acid functional group enables the formation of carbon-carbon bonds, making it valuable for creating aryl-aryl linkages in drug development and advanced materials. Additionally, it is employed in the synthesis of organic ele

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key reagent for constructing complex organic molecules, especially in the pharmaceutical and materials science industries. Its boronic acid functional group enables the formation of carbon-carbon bonds, making it valuable for creating aryl-aryl linkages in drug development and advanced materials. Additionally, it is employed in the synthesis of organic electronic materials, including polymers and small molecules used in OLEDs and other optoelectronic devices. Its ability to introduce aromatic structures into compounds makes it a versatile tool in designing molecules with specific electronic or photophysical properties.

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