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

95%

Reagent Code: #90325
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CAS Number 942610-02-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 388.27 g/mol
Formula C₂₃H₂₅BN₂O₃
badge Registry Numbers
MDL Number MFCD31561362
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in the development of pharmaceutical compounds and advanced materials. Its structure, featuring a urea linkage and a boronate ester group, makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in complex molecules. This reaction is essential in creating biologically active compounds, including potential drug candidates. Additionally, the naphthalene moiety in its structure can contribute to the development of fluorescent probes or sensors due to its inherent photophysical properties. Its applications extend to materials science, where it may be used in the synthesis of polymers or organic electronics, leveraging its stability and reactivity.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿5,265.00
inventory 250mg
10-20 days ฿21,276.00
1-(Naphthalen-1-yl)-1-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)urea
This chemical is primarily utilized in organic synthesis, particularly in the development of pharmaceutical compounds and advanced materials. Its structure, featuring a urea linkage and a boronate ester group, makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in complex molecules. This reaction is essential in creating biologically active compounds, including potential drug candidates. Additionally, the naphthalene moiety in its structure can contribute to the development of fluorescent probes or sensors due to its inherent photophysical properties. Its applications extend to materials science, where it may be used in the synthesis of polymers or organic electronics, leveraging its stability and reactivity.
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