N-(4-fluoro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-2-methoxyacetamide

95%

Reagent Code: #89704
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CAS Number 2246895-78-1

science Other reagents with same CAS 2246895-78-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 309.1409432 g/mol
Formula C₁₅H₂₁BFNO₄
badge Registry Numbers
MDL Number MFCD32206462
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This chemical is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceutical compounds. Its structure, featuring a boronate ester group, makes it a valuable intermediate in Suzuki-Miyaura cross-coupling reactions, which are widely employed to construct carbon-carbon bonds in drug discovery and material science. The presence of the fluorine atom enhances its potential as a building block for biologically active molecules, as fluorine is often incorporated into drugs to improve metabolic stability and binding affinity. Additionally, the methoxyacetamide moiety can contribute to the compound's solubility and interaction with biological targets, making it useful in the design of therapeutic agents.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿21,456.00
inventory 1g
10-20 days ฿55,800.00

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N-(4-fluoro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-2-methoxyacetamide
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This chemical is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceutical compounds. Its structure, featuring a boronate ester group, makes it a valuable intermediate in Suzuki-Miyaura cross-coupling reactions, which are widely employed to construct carbon-carbon bonds in drug discovery and material science. The presence of the fluorine atom enhances its potential as a building block for biologically active molecules, as fluorine is often incorporated into drugs to improve metabolic stability and binding affinity. Additionally, the methoxyacetamide moiety can contribute to the compound's solubility and interaction with biological targets, making it useful in the design of therapeutic agents.
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