tert-Butyl 6-chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-1-carboxylate
98%
Reagent
Code: #49740
CAS Number
1218790-24-9
blur_circular Chemical Specifications
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Molecular Information
Weight
377.6701 g/mol
Formula
C₁₉H₂₅BClNO₄
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Registry Numbers
MDL Number
MFCD15143606
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Storage & Handling
Storage
room temperature
description Product Description
This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester functional group makes it a valuable intermediate for constructing complex molecules, especially in pharmaceutical research and development. It is often employed in the synthesis of indole derivatives, which are crucial in drug discovery due to their biological activity. Additionally, it serves as a building block for creating compounds with potential applications in materials science and agrochemicals. Its stability and reactivity under mild conditions make it a preferred choice for chemists working on advanced synthetic routes.
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