2-Chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol
95%
Reagent
Code: #163788
CAS Number
1151564-17-8
blur_circular Chemical Specifications
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Molecular Information
Weight
254.52 g/mol
Formula
C₁₂H₁₆BClO₃
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Registry Numbers
MDL Number
MFCD16994269
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Storage & Handling
Storage
2-8°C, sealed, dry
description Product Description
Used primarily in cross-coupling reactions, this compound serves as a key intermediate in the synthesis of complex organic molecules, especially in pharmaceutical and agrochemical industries. Its boronate ester group enables Suzuki-Miyaura coupling, allowing efficient formation of carbon-carbon bonds. The presence of a phenolic hydroxyl group offers additional functionality for further chemical modifications, making it valuable in the development of functional materials, ligands, and bioactive compounds. Its stability and reactivity profile make it suitable for use in late-stage functionalization during drug discovery.
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