4,4,5,5-Tetramethyl-2-(5-nitronaphthalen-1-yl)-1,3,2-dioxaborolane
98%
Reagent
Code: #49281
CAS Number
885007-62-5
blur_circular Chemical Specifications
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Molecular Information
Weight
299.1294 g/mol
Formula
C₁₆H₁₈BNO₄
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Registry Numbers
MDL Number
MFCD25953902
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Storage & Handling
Storage
room temperature
description Product Description
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronate ester group makes it a valuable reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. It is often employed in the synthesis of pharmaceuticals, agrochemicals, and advanced materials, where precise molecular assembly is critical. Additionally, its nitronaphthalene moiety can contribute to the development of fluorescent or optoelectronic materials due to its potential electronic properties.
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