2-[3-(methoxymethyl)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
98%
Reagent
Code: #89621
CAS Number
675605-91-1
science Other reagents with same CAS 675605-91-1
blur_circular Chemical Specifications
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Molecular Information
Weight
248.13 g/mol
Formula
C₁₄H₂₁BO₃
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Registry Numbers
MDL Number
MFCD06795646
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Storage & Handling
Storage
room temperature, dry
description Product Description
This chemical is primarily utilized in organic synthesis as a key intermediate for the preparation of various complex molecules. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic ester reagent to form carbon-carbon bonds. This process is essential in the production of pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity make it a preferred choice for constructing biaryl compounds, which are foundational structures in many active pharmaceutical ingredients. Additionally, it is employed in the development of organic electronic materials, contributing to the creation of more efficient organic light-emitting diodes (OLEDs) and other electronic devices.
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