4-(tetramethyl-1,3,2-dioxaborolan-2-yl)naphthalene-1-carbonitrile
97%
Reagent
Code: #46246
CAS Number
1352794-90-1
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Molecular Information
Weight
279.1413 g/mol
Formula
C₁₇H₁₈BNO₂
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Registry Numbers
MDL Number
MFCD28167500
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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 the Suzuki-Miyaura reaction. Its boronate ester group acts as a key functional group, enabling the formation of carbon-carbon bonds with aryl or vinyl halides in the presence of a palladium catalyst. This makes it valuable in the production of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Additionally, its naphthalene core contributes to its use in the development of organic semiconductors and fluorescent dyes, where its structural properties enhance electronic and optical characteristics.
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