4,4,5,5-Tetramethyl-2-(2-(naphthalen-2-yl)phenyl)-1,3,2-dioxaborolane
≥95%
Reagent
Code: #118383
CAS Number
1062555-59-2
science Other reagents with same CAS 1062555-59-2
blur_circular Chemical Specifications
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Molecular Information
Weight
330.23 g/mol
Formula
C₂₂H₂₃BO₂
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Registry Numbers
MDL Number
MFCD22421637
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Storage & Handling
Storage
2-8°C, store under inert gas
description Product Description
This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex organic molecules, especially in the pharmaceutical and material science industries. Its boronate ester structure makes it a valuable reagent for forming carbon-carbon bonds, enabling the synthesis of biaryl compounds, which are essential in drug development and advanced materials. Additionally, it is utilized in the preparation of organic electronic materials, such as OLEDs and semiconductors, due to its ability to facilitate precise molecular design and functionalization.
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