1-(4-fluorobenzyl)-3-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)urea

95%

Reagent Code: #79980
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CAS Number 874301-88-9

science Other reagents with same CAS 874301-88-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 370.22556 g/mol
Formula C₂₀H₂₄BFN₂O₃
badge Registry Numbers
MDL Number MFCD22494690
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in the field of medicinal chemistry and drug development, particularly in the synthesis of biologically active molecules. Its structure, featuring a urea linkage and a boronate ester group, makes it a valuable intermediate in the preparation of targeted therapies, especially for diseases like cancer and inflammatory disorders. The boronate ester moiety is crucial for Suzuki-Miyaura cross-coupling reactions, a widely used method in organic synthesis to create complex molecules. Additionally, the presence of the fluorobenzyl group enhances the compound's ability to interact with biological targets, improving its potential as a precursor for developing enzyme inhibitors or receptor modulators. Its applications are also explored in the development of boron-containing drugs, which are gaining attention for their therapeutic potential.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿5,292.00
inventory 250mg
10-20 days ฿21,150.00

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1-(4-fluorobenzyl)-3-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)urea
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This compound is primarily utilized in the field of medicinal chemistry and drug development, particularly in the synthesis of biologically active molecules. Its structure, featuring a urea linkage and a boronate ester group, makes it a valuable intermediate in the preparation of targeted therapies, especially for diseases like cancer and inflammatory disorders. The boronate ester moiety is crucial for Suzuki-Miyaura cross-coupling reactions, a widely used method in organic synthesis to create complex mo

This compound is primarily utilized in the field of medicinal chemistry and drug development, particularly in the synthesis of biologically active molecules. Its structure, featuring a urea linkage and a boronate ester group, makes it a valuable intermediate in the preparation of targeted therapies, especially for diseases like cancer and inflammatory disorders. The boronate ester moiety is crucial for Suzuki-Miyaura cross-coupling reactions, a widely used method in organic synthesis to create complex molecules. Additionally, the presence of the fluorobenzyl group enhances the compound's ability to interact with biological targets, improving its potential as a precursor for developing enzyme inhibitors or receptor modulators. Its applications are also explored in the development of boron-containing drugs, which are gaining attention for their therapeutic potential.

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