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

97%

Reagent Code: #116975
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CAS Number 1288978-82-4

science Other reagents with same CAS 1288978-82-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 267.06 g/mol
Formula C₁₂H₁₅BFNO₄
badge Registry Numbers
MDL Number MFCD16996295
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 key intermediate for constructing complex organic molecules, especially in pharmaceutical research and development. The compound’s boronate ester group makes it valuable for introducing aryl or heteroaryl groups into target molecules, enabling the creation of biologically active compounds. It is also utilized in the development of materials science applications, such as organic electronics and advanced polymers, due to its ability to form stable carbon-carbon bonds. Additionally, it plays a role in the synthesis of agrochemicals and fine chemicals, contributing to the production of pesticides, herbicides, and other specialized chemical products.

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Test Parameter Specification
Appearance White to Yellow Crystalline powder or Solid
Purity (%) 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿29,358.00
inventory 250mg
10-20 days ฿2,880.00
inventory 1g
10-20 days ฿7,290.00

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2-(4-Fluoro-2-nitrophenyl)-4,4,5,5-tetramethyl-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 key intermediate for constructing complex organic molecules, especially in pharmaceutical research and development. The compound’s boronate ester group makes it valuable for introducing aryl or heteroaryl groups into target molecules, enabling the creation of biologically active compounds. It is also utilized in the development of materials science applications, such as organic el

This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex organic molecules, especially in pharmaceutical research and development. The compound’s boronate ester group makes it valuable for introducing aryl or heteroaryl groups into target molecules, enabling the creation of biologically active compounds. It is also utilized in the development of materials science applications, such as organic electronics and advanced polymers, due to its ability to form stable carbon-carbon bonds. Additionally, it plays a role in the synthesis of agrochemicals and fine chemicals, contributing to the production of pesticides, herbicides, and other specialized chemical products.

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