1H-indol-5-yl-5-boronic acid

≥95%

Reagent Code: #90877
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CAS Number 144104-59-6

science Other reagents with same CAS 144104-59-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 160.97 g/mol
Formula C₈H₈BNO₂
badge Registry Numbers
MDL Number MFCD01319013
inventory_2 Storage & Handling
Storage 2~8℃

description Product Description

This compound is widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key building block for creating complex organic molecules. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the pharmaceutical industry for synthesizing drug candidates and bioactive compounds. Additionally, it is employed in material science for developing organic electronic materials, such as OLEDs and conductive polymers, due to its ability to introduce indole moieties into larger molecular frameworks. Its versatility also extends to agrochemical research, where it aids in the design of novel pesticides and herbicides.

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Test Parameter Specification
Appearance White to orange to brown crystal to powder
Purity 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿760.00
inventory 5g
10-20 days ฿2,980.00
inventory 25g
10-20 days ฿10,260.00

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1H-indol-5-yl-5-boronic acid
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This compound is widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key building block for creating complex organic molecules. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the pharmaceutical industry for synthesizing drug candidates and bioactive compounds. Additionally, it is employed in material science for developing organic electronic ma

This compound is widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key building block for creating complex organic molecules. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the pharmaceutical industry for synthesizing drug candidates and bioactive compounds. Additionally, it is employed in material science for developing organic electronic materials, such as OLEDs and conductive polymers, due to its ability to introduce indole moieties into larger molecular frameworks. Its versatility also extends to agrochemical research, where it aids in the design of novel pesticides and herbicides.

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