2-[4-(2-bromoethoxy)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

95%

Reagent Code: #90363
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CAS Number 913836-27-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 327.0218 g/mol
Formula C₁₄H₂₀BBrO₃
badge Registry Numbers
MDL Number MFCD09027285
thermostat Physical Properties
Melting Point 90-92 °C
Boiling Point 391.9 °C at 760 mmHg
inventory_2 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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Size Availability Unit Price Quantity
inventory 250mg
10-20 days $45.58
inventory 1g
10-20 days $96.54
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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