2-(4-(Benzyloxy)-2-ethyl-5-fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

95%

Reagent Code: #124018
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CAS Number 1825308-37-9

science Other reagents with same CAS 1825308-37-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 356.24 g/mol
Formula C₂₁H₂₆BFO₃
badge Registry Numbers
MDL Number MFCD31803617
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are pivotal in forming carbon-carbon bonds. Its boronate ester group acts as a key intermediate, enabling the coupling of aryl or vinyl halides with aryl or vinyl boronic acids. This reaction is widely employed in the pharmaceutical industry for the synthesis of complex molecules, including drug candidates. Additionally, it finds application in material science for the development of organic electronic materials, such as polymers and small molecules used in organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). The compound's stability and reactivity make it a valuable tool in advanced chemical research and industrial processes.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿13,671.00
inventory 1g
10-20 days ฿27,342.00
inventory 100mg
10-20 days ฿7,290.00

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2-(4-(Benzyloxy)-2-ethyl-5-fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are pivotal in forming carbon-carbon bonds. Its boronate ester group acts as a key intermediate, enabling the coupling of aryl or vinyl halides with aryl or vinyl boronic acids. This reaction is widely employed in the pharmaceutical industry for the synthesis of complex molecules, including drug candidates. Additionally, it finds application in material science for the development of o

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are pivotal in forming carbon-carbon bonds. Its boronate ester group acts as a key intermediate, enabling the coupling of aryl or vinyl halides with aryl or vinyl boronic acids. This reaction is widely employed in the pharmaceutical industry for the synthesis of complex molecules, including drug candidates. Additionally, it finds application in material science for the development of organic electronic materials, such as polymers and small molecules used in organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). The compound's stability and reactivity make it a valuable tool in advanced chemical research and industrial processes.

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