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

≥95%

Reagent Code: #115713
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CAS Number 887757-48-4

science Other reagents with same CAS 887757-48-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 270.08 g/mol
Formula C₁₃H₁₇BF₂O₃
badge Registry Numbers
MDL Number MFCD09878543
thermostat Physical Properties
Boiling Point 319.3±37.0°C at 760 mmHg
inventory_2 Storage & Handling
Density 1.134g/cm3
Storage 2-8°C, store under inert gas

description Product Description

This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex organic molecules, especially in the pharmaceutical industry. Its boronate ester group facilitates the formation of carbon-carbon bonds, making it valuable in the development of drugs, agrochemicals, and advanced materials. Additionally, it is employed in the synthesis of biologically active compounds and functional materials due to its stability and reactivity under mild conditions.

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Test Parameter Specification
Appearance White Solid
Purity (%) 95-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,664.00
inventory 250mg
10-20 days ฿1,188.00
inventory 5g
10-20 days ฿10,701.00

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2-(4-(Difluoromethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex organic molecules, especially in the pharmaceutical industry. Its boronate ester group facilitates the formation of carbon-carbon bonds, making it valuable in the development of drugs, agrochemicals, and advanced materials. Additionally, it is employed in the synthesis of biologically active compounds and functional materials due to its st

This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex organic molecules, especially in the pharmaceutical industry. Its boronate ester group facilitates the formation of carbon-carbon bonds, making it valuable in the development of drugs, agrochemicals, and advanced materials. Additionally, it is employed in the synthesis of biologically active compounds and functional materials due to its stability and reactivity under mild conditions.

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