(1-(tert-Butoxycarbonyl)-6-fluoro-1H-indol-2-yl)boronic acid
98%
Reagent
Code: #39715
CAS Number
1000068-26-7
blur_circular Chemical Specifications
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Molecular Information
Weight
279.0700 g/mol
Formula
C₁₃H₁₅BFNO₄
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Registry Numbers
MDL Number
MFCD09953519
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Storage & Handling
Storage
room temperature
description Product Description
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate in the production of complex molecules, especially in pharmaceutical research. Its boronic acid group enables it to form carbon-carbon bonds efficiently, making it valuable for constructing indole-based compounds. These compounds are often explored for their potential biological activities, including drug development for treating various diseases. Additionally, the tert-butoxycarbonyl (Boc) protecting group allows for selective deprotection, facilitating controlled synthesis processes.
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