Diethyl(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)phosphonate
95%
Reagent
Code: #132387
CAS Number
914656-92-1
blur_circular Chemical Specifications
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Molecular Information
Weight
340.16 g/mol
Formula
C₁₆H₂₆BO₅P
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Registry Numbers
MDL Number
MFCD31727724
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Storage & Handling
Storage
Room temperature
description Product Description
Used primarily in organic synthesis as a key reagent for cross-coupling reactions, enabling the formation of carbon–phosphorus and carbon–carbon bonds. Its boronate ester group facilitates Suzuki-Miyaura coupling, allowing efficient construction of biaryl and heterobiaryl systems important in pharmaceuticals and agrochemicals. The phosphonate moiety adds versatility for further functionalization or as a precursor to phosphate mimics in bioactive molecules. Commonly employed in the development of novel therapeutic agents and functional materials due to its dual reactivity.
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