2-(2-Fluoro-6-methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

97%

Reagent Code: #62292
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CAS Number 1599432-41-3

science Other reagents with same CAS 1599432-41-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 252.09 g/mol
Formula C₁₃H₁₈BFO₃
badge Registry Numbers
MDL Number MFCD16996294
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

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, which is crucial in the development of pharmaceuticals, agrochemicals, and advanced materials. Its fluorine and methoxy substituents enhance its reactivity and selectivity, making it valuable in constructing complex organic molecules. Additionally, it is employed in the synthesis of heterocyclic compounds and as an intermediate in the production of bioactive molecules, contributing to drug discovery and material science research.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿1,359.00
1g
10-20 days ฿3,384.00
5g
10-20 days ฿13,527.00
2-(2-Fluoro-6-methoxyphenyl)-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, which is crucial in the development of pharmaceuticals, agrochemicals, and advanced materials. Its fluorine and methoxy substituents enhance its reactivity and selectivity, making it valuable in constructing complex organic molecules. Additionally, it is employed in the synthesis of heterocy

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, which is crucial in the development of pharmaceuticals, agrochemicals, and advanced materials. Its fluorine and methoxy substituents enhance its reactivity and selectivity, making it valuable in constructing complex organic molecules. Additionally, it is employed in the synthesis of heterocyclic compounds and as an intermediate in the production of bioactive molecules, contributing to drug discovery and material science research.

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