2-4-[(4-chlorophenyl)methoxy]phenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

95%

Reagent Code: #83803
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CAS Number 2246937-34-6

science Other reagents with same CAS 2246937-34-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 344.64018 g/mol
Formula C₁₉H₂₂BClO₃
badge Registry Numbers
MDL Number MFCD31583310
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in organic synthesis as a versatile building block for the preparation of more complex molecules. Its boronic ester functional group makes it particularly valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. This reaction is essential in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. The compound’s structure, featuring a chlorophenyl group, also allows it to serve as an intermediate in the development of biologically active compounds, including potential drug candidates targeting specific receptors or enzymes. Additionally, its stability and reactivity make it a useful reagent in the design of organic electronic materials, such as those used in OLEDs or organic photovoltaics.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿9,270.00
inventory 100mg
10-20 days ฿27,720.00

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2-4-[(4-chlorophenyl)methoxy]phenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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This compound is primarily utilized in organic synthesis as a versatile building block for the preparation of more complex molecules. Its boronic ester functional group makes it particularly valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. This reaction is essential in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. The compound’s structure, featuring a chlorophenyl group, also allows it to serve as an intermediate in the development of biologically active compounds, including potential drug candidates targeting specific receptors or enzymes. Additionally, its stability and reactivity make it a useful reagent in the design of organic electronic materials, such as those used in OLEDs or organic photovoltaics.
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