2-(3-Methoxy-5-(trifluoromethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
97%
Reagent
Code: #115694
CAS Number
479411-93-3
science Other reagents with same CAS 479411-93-3
blur_circular Chemical Specifications
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Molecular Information
Weight
302.10 g/mol
Formula
C₁₄H₁₈BF₃O₃
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Registry Numbers
MDL Number
MFCD11846463
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Physical Properties
Boiling Point
340.4±42.0°C at 760 mmHg
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Storage & Handling
Storage
2-8°C, dry and sealed
description Product Description
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a boronic ester reagent, enabling the formation of carbon-carbon bonds, which is crucial in the development of pharmaceuticals, agrochemicals, and advanced materials. Its trifluoromethyl and methoxy groups enhance its reactivity and selectivity, making it valuable in the synthesis of complex organic molecules. Additionally, it is employed in the preparation of bioactive compounds and intermediates for drug discovery, contributing to the development of new therapeutic agents.
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