2-[4-(2-bromoethoxy)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
95%
Reagent
Code: #90363
CAS Number
913836-27-8
blur_circular Chemical Specifications
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Molecular Information
Weight
327.0218 g/mol
Formula
C₁₄H₂₀BBrO₃
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Registry Numbers
MDL Number
MFCD09027285
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Physical Properties
Melting Point
90-92 °C
Boiling Point
391.9 °C at 760 mmHg
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Storage & Handling
Density
1.27 g/cm3
Storage
2-8°C
description Product Description
This chemical is primarily utilized in organic synthesis as a key intermediate for the preparation of more complex molecules. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the pharmaceutical and materials science industries to construct carbon-carbon bonds. The boronate ester group in the compound facilitates the coupling process, enabling the formation of biaryl structures, which are essential in the development of drugs, agrochemicals, and organic electronic materials. Additionally, its bromoethoxy group allows for further functionalization, making it versatile in designing targeted molecules for specific applications.
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2-[4-(2-bromoethoxy)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
This chemical is primarily utilized in organic synthesis as a key intermediate for the preparation of more complex molecules. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the pharmaceutical and materials science industries to construct carbon-carbon bonds. The boronate ester group in the compound facilitates the coupling process, enabling the formation of biaryl structures, which are essential in the development of drugs, agrochemicals, and organic electronic materials. Additionally, its bromoethoxy group allows for further functionalization, making it versatile in designing targeted molecules for specific applications.
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