1-(Methylsulfonyl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)indoline
95%
Reagent
Code: #39655
CAS Number
1132944-44-5
blur_circular Chemical Specifications
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Molecular Information
Weight
323.2155 g/mol
Formula
C₁₅H₂₂BNO₄S
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Registry Numbers
MDL Number
MFCD28718122
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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, where it acts as a key intermediate. Its boronate ester group enables the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, it is employed in the development of bioactive compounds and materials science for creating advanced polymers and functional materials. Its stability and reactivity under mild conditions make it a preferred choice in medicinal chemistry for drug discovery and development.
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