N-(2-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)butyramide

95%

Reagent Code: #83679
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CAS Number 2246585-78-2

science Other reagents with same CAS 2246585-78-2

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Weight 319.20364 g/mol
Formula C₁₇H₂₆BNO₄
inventory_2 Storage & Handling
Storage 2-8°C

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 group serves as a key functional group, enabling the formation of carbon-carbon bonds, which is essential in constructing complex organic molecules. It is often employed in the development of pharmaceuticals, agrochemicals, and advanced materials, where precise molecular assembly is required. Additionally, its methoxy and amide groups contribute to its stability and reactivity, making it a valuable intermediate in medicinal chemistry for designing drug candidates with improved efficacy and selectivity.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿3,672.00
inventory 100mg
10-20 days ฿10,998.00

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N-(2-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)butyramide
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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 group serves as a key functional group, enabling the formation of carbon-carbon bonds, which is essential in constructing complex organic molecules. It is often employed in the development of pharmaceuticals, agrochemicals, and advanced materials, where precise molecular assembly is required. Additionally, its methoxy and amide groups contribute to its

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester group serves as a key functional group, enabling the formation of carbon-carbon bonds, which is essential in constructing complex organic molecules. It is often employed in the development of pharmaceuticals, agrochemicals, and advanced materials, where precise molecular assembly is required. Additionally, its methoxy and amide groups contribute to its stability and reactivity, making it a valuable intermediate in medicinal chemistry for designing drug candidates with improved efficacy and selectivity.

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