4,4,5,5-Tetramethyl-2-(3-(trifluoromethyl)benzyl)-1,3,2-dioxaborolane

≥95%

Reagent Code: #66326
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CAS Number 1190235-39-2

science Other reagents with same CAS 1190235-39-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 286.10 g/mol
Formula C₁₄H₁₈BF₃O₂
badge Registry Numbers
MDL Number MFCD10698528
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a boronic ester reagent, enabling the formation of carbon-carbon bonds between aryl or vinyl boronic acids and aryl or vinyl halides. Its stability and reactivity make it valuable in constructing complex organic molecules, such as pharmaceuticals, agrochemicals, and advanced materials. The trifluoromethyl group enhances its electron-withdrawing properties, improving its efficiency in catalytic processes. Additionally, it is employed in the development of boron-containing compounds for medicinal chemistry and material science research.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿4,995.00
1g
10-20 days ฿12,492.00
5g
10-20 days ฿45,072.00
4,4,5,5-Tetramethyl-2-(3-(trifluoromethyl)benzyl)-1,3,2-dioxaborolane
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This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a boronic ester reagent, enabling the formation of carbon-carbon bonds between aryl or vinyl boronic acids and aryl or vinyl halides. Its stability and reactivity make it valuable in constructing complex organic molecules, such as pharmaceuticals, agrochemicals, and advanced materials. The trifluoromethyl group enhances its electron-withdrawing properties, improving its efficiency i

This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a boronic ester reagent, enabling the formation of carbon-carbon bonds between aryl or vinyl boronic acids and aryl or vinyl halides. Its stability and reactivity make it valuable in constructing complex organic molecules, such as pharmaceuticals, agrochemicals, and advanced materials. The trifluoromethyl group enhances its electron-withdrawing properties, improving its efficiency in catalytic processes. Additionally, it is employed in the development of boron-containing compounds for medicinal chemistry and material science research.

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