4,4,5,5-Tetramethyl-2-(4-((trifluoromethyl)sulfonyl)phenyl)-1,3,2-dioxaborolane
97%
Reagent
Code: #244476
CAS Number
648904-89-6
science Other reagents with same CAS 648904-89-6
blur_circular Chemical Specifications
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Molecular Information
Weight
336.13 g/mol
Formula
C₁₃H₁₆BF₃O₄S
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Registry Numbers
MDL Number
MFCD28969495
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Storage & Handling
Storage
2-8°C
description Product Description
Widely used in cross-coupling reactions, this compound serves as a key boronic ester reagent in Suzuki-Miyaura coupling, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its electron-deficient aryl group enhances reactivity and stability, making it valuable for constructing complex aromatic systems. It is particularly useful in late-stage functionalization due to its tolerance of various functional groups and compatibility with palladium catalysts. Additionally, it acts as a building block in materials science for designing organic electronic materials and conjugated polymers.
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