2-(Tetramethyl-1,3,2-dioxaborolan-2-yl)prop-2-en-1-ol
95%
Reagent
Code: #243298
CAS Number
1294009-05-4
blur_circular Chemical Specifications
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Molecular Information
Weight
184.04 g/mol
Formula
C₉H₁₇BO₃
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Registry Numbers
MDL Number
MFCD31559666
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Storage & Handling
Storage
Room temperature, inert gas
description Product Description
Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its allylic alcohol and boronate ester functionalities allow for versatile transformations, including the preparation of complex organic molecules with high selectivity. Commonly employed in the development of bioactive compounds and functional materials due to its reactivity and stability under various coupling conditions.
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