N-(2-chloro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclopropanecarboxamide

95%

Reagent Code: #83924
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CAS Number 2246786-07-0

science Other reagents with same CAS 2246786-07-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 321.60684 g/mol
Formula C₁₆H₂₁BClNO₃
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical 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 moiety, enabling the formation of 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, where precise molecular architecture is crucial. Additionally, it finds applications in material science for the synthesis of advanced polymers and organic electronic materials. Its cyclopropane moiety can impart unique steric and electronic properties to the final product, making it valuable in designing compounds with specific functionalities.

Available Sizes & Pricing

Size Availability Unit Price Quantity
25mg
10-20 days ฿3,672.00
100mg
10-20 days ฿10,998.00
N-(2-chloro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclopropanecarboxamide
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This chemical 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 moiety, enabling the formation of 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, where precise molecular architecture is crucial. Additionally, it finds applications in material science for the

This chemical 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 moiety, enabling the formation of 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, where precise molecular architecture is crucial. Additionally, it finds applications in material science for the synthesis of advanced polymers and organic electronic materials. Its cyclopropane moiety can impart unique steric and electronic properties to the final product, making it valuable in designing compounds with specific functionalities.

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