Dibenzo[b,d]thiophen-2-ylboronic acid

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Reagent Code: #91097
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CAS Number 668983-97-9

science Other reagents with same CAS 668983-97-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 228.08 g/mol
Formula C₁₂H₉BO₂S
thermostat Physical Properties
Boiling Point 480.2°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create complex organic compounds. It serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and organic materials. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in constructing carbon-carbon bonds. Additionally, it is employed in the development of organic electronic materials, such as OLEDs and semiconductors, due to its ability to modify electronic properties. Its versatility also extends to polymer chemistry, where it aids in the synthesis of functionalized polymers.

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Test Parameter Specification
Appearance white to off-white solid
Purity 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,680.00
inventory 1g
10-20 days ฿390.00
inventory 25g
10-20 days ฿4,600.00

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Dibenzo[b,d]thiophen-2-ylboronic acid
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Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create complex organic compounds. It serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and organic materials. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in constructing carbon-carbon bonds. Additionally, it is employed in the development of organic electronic materials, such as OLEDs and semiconductors, due to its ability to modify electronic

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create complex organic compounds. It serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and organic materials. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in constructing carbon-carbon bonds. Additionally, it is employed in the development of organic electronic materials, such as OLEDs and semiconductors, due to its ability to modify electronic properties. Its versatility also extends to polymer chemistry, where it aids in the synthesis of functionalized polymers.

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