Methyl 4,5-dimethoxy-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate

96%

Reagent Code: #87411
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CAS Number 420166-80-4

science Other reagents with same CAS 420166-80-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 322.16 g/mol
Formula C₁₆H₂₃BO₆
badge Registry Numbers
MDL Number MFCD16036165
thermostat Physical Properties
Boiling Point 440.1±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.13±0.1 g/cm3(Predicted)
Storage 2-8°C, inert gas

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 functional group makes it a valuable reagent for forming carbon-carbon bonds, which is essential in constructing complex organic molecules. It is often employed in the pharmaceutical industry for the development of drug candidates, enabling the introduction of aromatic or heteroaromatic structures into target molecules. Additionally, it is used in material science for the synthesis of advanced polymers and organic electronic materials, where precise molecular architecture is crucial. Its stability and reactivity under mild conditions make it a preferred choice in various catalytic processes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,971.00
inventory 250mg
10-20 days ฿3,339.00
inventory 1g
10-20 days ฿9,000.00

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Methyl 4,5-dimethoxy-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester functional group makes it a valuable reagent for forming carbon-carbon bonds, which is essential in constructing complex organic molecules. It is often employed in the pharmaceutical industry for the development of drug candidates, enabling the introduction of aromatic or heteroaromatic structures into target molecules. Additionally, it is used in materia
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester functional group makes it a valuable reagent for forming carbon-carbon bonds, which is essential in constructing complex organic molecules. It is often employed in the pharmaceutical industry for the development of drug candidates, enabling the introduction of aromatic or heteroaromatic structures into target molecules. Additionally, it is used in material science for the synthesis of advanced polymers and organic electronic materials, where precise molecular architecture is crucial. Its stability and reactivity under mild conditions make it a preferred choice in various catalytic processes.
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