2-(3-Methoxy-5-(trifluoromethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

97%

Reagent Code: #115694
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CAS Number 479411-93-3

science Other reagents with same CAS 479411-93-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 302.10 g/mol
Formula C₁₄H₁₈BF₃O₃
badge Registry Numbers
MDL Number MFCD11846463
thermostat Physical Properties
Boiling Point 340.4±42.0°C at 760 mmHg
inventory_2 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.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,241.00
inventory 5g
10-20 days ฿9,108.00
inventory 10g
10-20 days ฿15,291.00

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2-(3-Methoxy-5-(trifluoromethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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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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