(1-(tert-Butoxycarbonyl)-5-((tert-butoxycarbonyl)amino)-1H-indol-2-yl)boronic acid
≥95%
Reagent
Code: #113003
CAS Number
913388-66-6
science Other reagents with same CAS 913388-66-6
blur_circular Chemical Specifications
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Molecular Information
Weight
376.21 g/mol
Formula
C₁₈H₂₅BN₂O₆
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Registry Numbers
MDL Number
MFCD11616305
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Storage & Handling
Density
1.2g/cm3
Storage
2-8°C, store under inert gas
description Product Description
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a key intermediate in the preparation of complex molecules, including pharmaceuticals and agrochemicals. The presence of boronic acid and Boc-protected amino groups makes it valuable for constructing indole-based structures, which are common in bioactive compounds. Its stability and reactivity under mild conditions allow for efficient use in medicinal chemistry research, enabling the development of new drug candidates. Additionally, it is employed in the synthesis of advanced materials and polymers, where precise molecular architecture is required.
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