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

95%

Reagent Code: #42230
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CAS Number 2246838-42-4

science Other reagents with same CAS 2246838-42-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 344.64 g/mol
Formula C₁₉H₂₂BClO₃
badge Registry Numbers
MDL Number MFCD31916451
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in organic synthesis as a key intermediate in the preparation of various biologically active molecules. Its boronate ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the pharmaceutical industry to construct complex organic compounds, including drug candidates. Additionally, it serves as a building block in the development of materials with potential applications in optoelectronics and organic light-emitting diodes (OLEDs). Its stability and reactivity under mild conditions make it a preferred choice for researchers working on the synthesis of novel organic frameworks and polymers.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿7,785.00
inventory 1g
10-20 days ฿22,500.00

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2-3-[(3-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 key intermediate in the preparation of various biologically active molecules. Its boronate ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the pharmaceutical industry to construct complex organic compounds, including drug candidates. Additionally, it serves as a building block in the development of materials with potential applications in optoelectronics and organic light-emitti

This compound is primarily utilized in organic synthesis as a key intermediate in the preparation of various biologically active molecules. Its boronate ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the pharmaceutical industry to construct complex organic compounds, including drug candidates. Additionally, it serves as a building block in the development of materials with potential applications in optoelectronics and organic light-emitting diodes (OLEDs). Its stability and reactivity under mild conditions make it a preferred choice for researchers working on the synthesis of novel organic frameworks and polymers.

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