2-(4-(3,4-Difluorophenyl)thiophen-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

95%

Reagent Code: #89625
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CAS Number 1402227-89-7

science Other reagents with same CAS 1402227-89-7

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scatter_plot Molecular Information
Weight 322.18 g/mol
Formula C₁₆H₁₇BF₂O₂S
badge Registry Numbers
MDL Number MFCD18436139
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a boronic ester reagent, enabling the formation of carbon-carbon bonds between aryl or heteroaryl groups. This makes it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity under mild conditions make it a preferred choice for constructing complex organic molecules. Additionally, it is used in the development of organic electronic materials, including OLEDs and semiconductors, due to its ability to facilitate precise molecular design.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿8,280.00
inventory 25mg
10-20 days ฿24,300.00

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2-(4-(3,4-Difluorophenyl)thiophen-2-yl)-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 Suzuki-Miyaura coupling. It serves as a boronic ester reagent, enabling the formation of carbon-carbon bonds between aryl or heteroaryl groups. This makes it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity under mild conditions make it a preferred choice for constructing complex organic molecules. Additionally, it is used in the development of organic electronic materials, including OLEDs and semiconductors, due to its ability to facilitate precise molecular design.
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