4,4,5,5-Tetramethyl-2-(3-phenoxyphenyl)-1,3,2-dioxaborolane

≥95%

Reagent Code: #118369
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CAS Number 864772-18-9

science Other reagents with same CAS 864772-18-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 296.17 g/mol
Formula C₁₈H₂₁BO₃
badge Registry Numbers
MDL Number MFCD11973622
thermostat Physical Properties
Boiling Point 402.8±28.0°C at 760 mmHg
inventory_2 Storage & Handling
Density 1.09g/cm3
Storage 2-8°C, dry and sealed

description Product Description

This chemical is primarily used in organic synthesis as a versatile intermediate, particularly in Suzuki-Miyaura cross-coupling reactions. It facilitates the formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronate ester structure enhances stability and reactivity, enabling efficient coupling with aryl halides. Additionally, it is employed in the development of organic light-emitting diodes (OLEDs) and other electronic materials due to its ability to create complex aromatic structures. Its application in medicinal chemistry includes the synthesis of bioactive compounds and drug candidates.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,528.00
inventory 1g
10-20 days ฿8,802.00
inventory 100mg
10-20 days ฿2,358.00

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4,4,5,5-Tetramethyl-2-(3-phenoxyphenyl)-1,3,2-dioxaborolane
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This chemical is primarily used in organic synthesis as a versatile intermediate, particularly in Suzuki-Miyaura cross-coupling reactions. It facilitates the formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronate ester structure enhances stability and reactivity, enabling efficient coupling with aryl halides. Additionally, it is employed in the development of organic light-emitting diodes (OLEDs) and other electronic

This chemical is primarily used in organic synthesis as a versatile intermediate, particularly in Suzuki-Miyaura cross-coupling reactions. It facilitates the formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronate ester structure enhances stability and reactivity, enabling efficient coupling with aryl halides. Additionally, it is employed in the development of organic light-emitting diodes (OLEDs) and other electronic materials due to its ability to create complex aromatic structures. Its application in medicinal chemistry includes the synthesis of bioactive compounds and drug candidates.

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