tert-Butyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-thioxanthen-2-ylcarbamate
95%
Reagent
Code: #150517
CAS Number
587871-47-4
blur_circular Chemical Specifications
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Molecular Information
Weight
439.38 g/mol
Formula
C₂₄H₃₀BNO₄S
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Registry Numbers
MDL Number
MFCD30469041
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Storage & Handling
Storage
Room temperature, sealed, dry
description Product Description
Used in organic synthesis as a key intermediate for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its boronate ester group facilitates palladium-catalyzed coupling with aryl halides, making it valuable in constructing complex aromatic systems. The carbamate-protected amine allows for selective deprotection and further functionalization in multi-step synthesis. Commonly applied in the preparation of functional materials and bioactive molecules where thioxanthene scaffolds are required.
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