N-3-pyridinyl-N'-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]Urea

95%

Reagent Code: #60828
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CAS Number 874298-19-8

science Other reagents with same CAS 874298-19-8

blur_circular Chemical Specifications

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Weight 339.19658 g/mol
Formula C₁₈H₂₂BN₃O₃
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 design of kinase inhibitors. It serves as a key intermediate in the synthesis of targeted therapies, especially for cancer treatment. The boronate ester functional group allows for versatile chemical transformations, making it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely used to construct complex molecules in pharmaceutical research. Additionally, its urea moiety contributes to hydrogen bonding interactions, enhancing its potential as a bioactive molecule in drug discovery efforts.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿5,391.00
inventory 250mg
10-20 days ฿21,582.00

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N-3-pyridinyl-N'-[4-(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 design of kinase inhibitors. It serves as a key intermediate in the synthesis of targeted therapies, especially for cancer treatment. The boronate ester functional group allows for versatile chemical transformations, making it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely used to construct complex molecules in pharmaceutical research. Additionally, its urea moiety cont

This compound is primarily utilized in the field of medicinal chemistry and drug development, particularly in the design of kinase inhibitors. It serves as a key intermediate in the synthesis of targeted therapies, especially for cancer treatment. The boronate ester functional group allows for versatile chemical transformations, making it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely used to construct complex molecules in pharmaceutical research. Additionally, its urea moiety contributes to hydrogen bonding interactions, enhancing its potential as a bioactive molecule in drug discovery efforts.

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