(1-(tert-Butoxycarbonyl)-6-cyano-1H-indol-2-yl)boronic acid
98%
Reagent
Code: #39716
CAS Number
913835-67-3
blur_circular Chemical Specifications
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Molecular Information
Weight
286.0900 g/mol
Formula
C₁₄H₁₅BN₂O₄
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Registry Numbers
MDL Number
MFCD08436056
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Physical Properties
Boiling Point
509.1 °C at 760 mmHg
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Storage & Handling
Density
1.21g/cm3
Storage
-20°C
description Product Description
This chemical is primarily used in organic synthesis, particularly in the preparation of complex molecules through cross-coupling reactions. It serves as a key intermediate in the development of pharmaceuticals, especially in the synthesis of indole-based compounds, which are important in drug discovery. The boronic acid group enables it to participate in Suzuki-Miyaura coupling reactions, a widely used method for forming carbon-carbon bonds. Additionally, the tert-butoxycarbonyl (Boc) protecting group allows for selective deprotection during multi-step synthesis, making it valuable in the construction of biologically active molecules. Its applications are particularly relevant in the production of potential therapeutic agents targeting various diseases.
format_list_bulleted Product Specification
| Test Parameter | Specification |
|---|---|
| Appearance | Solid |
| Purity (%) | 97.5-100 |
| NMR | Conforms to Structure |
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