Benzyl (2-fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)carbamate
95%
Reagent
Code: #152235
CAS Number
1256359-14-4
blur_circular Chemical Specifications
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Molecular Information
Weight
371.21 g/mol
Formula
C₂₀H₂₃BFNO₄
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Registry Numbers
MDL Number
MFCD17015818
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Storage & Handling
Storage
Room temperature, inert gas
description Product Description
Used as an intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. The boronate ester group enables efficient carbon-carbon bond formation, while the benzyl carbamate acts as a protecting group for amines, allowing selective functionalization in multi-step syntheses. Commonly applied in the development of bioactive compounds and functional materials requiring precise molecular architecture.
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