1-(Naphthalen-1-yl)-1-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)urea
95%
Reagent
Code: #90325
CAS Number
942610-02-8
blur_circular Chemical Specifications
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Molecular Information
Weight
388.27 g/mol
Formula
C₂₃H₂₅BN₂O₃
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Registry Numbers
MDL Number
MFCD31561362
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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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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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