1-benzyl-3-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]urea

95%

Reagent Code: #90050
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CAS Number 874299-02-2

science Other reagents with same CAS 874299-02-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 352.2351 g/mol
Formula C₂₀H₂₅BN₂O₃
badge Registry Numbers
MDL Number MFCD22494564
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. It serves as a key intermediate in the synthesis of biologically active molecules, particularly those targeting protein kinases and other enzymes involved in disease pathways. Its boronic ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, enabling the construction of complex organic frameworks. Additionally, it is employed in the development of potential therapeutic agents for conditions such as cancer, inflammation, and neurodegenerative disorders. Its structural features, including the benzyl and phenyl urea moieties, allow for precise modifications, enhancing drug efficacy and selectivity.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿4,572.00
inventory 250mg
10-20 days ฿18,180.00

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1-benzyl-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. It serves as a key intermediate in the synthesis of biologically active molecules, particularly those targeting protein kinases and other enzymes involved in disease pathways. Its boronic ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, enabling the construction of complex organic frameworks. Additionally, it is employed in the development of potential therapeutic agents for c

This compound is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of biologically active molecules, particularly those targeting protein kinases and other enzymes involved in disease pathways. Its boronic ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, enabling the construction of complex organic frameworks. Additionally, it is employed in the development of potential therapeutic agents for conditions such as cancer, inflammation, and neurodegenerative disorders. Its structural features, including the benzyl and phenyl urea moieties, allow for precise modifications, enhancing drug efficacy and selectivity.

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