2-Methyl-4-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)thiazole
≥95%
Reagent
Code: #132268
CAS Number
857283-68-2
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Molecular Information
Weight
301.21 g/mol
Formula
C₁₆H₂₀BNO₂S
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Registry Numbers
MDL Number
MFCD08060513
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Storage & Handling
Storage
Room temperature
description Product Description
Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, as a key intermediate for constructing biaryl compounds. Its boronate ester group enables efficient carbon-carbon bond formation, making it valuable in pharmaceutical and agrochemical research for developing complex aromatic molecules. Commonly applied in the preparation of functional materials, including organic semiconductors and luminescent compounds. Its thiazole core contributes to electron-transport properties, useful in OLEDs and other electronic devices. Stable and compatible with a wide range of reaction conditions, it supports high-yield transformations in both academic and industrial settings.
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