N-Cyclopropyl-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetamide

96%

Reagent Code: #121509
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CAS Number 1031747-36-0

science Other reagents with same CAS 1031747-36-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 301.19 g/mol
Formula C₁₇H₂₄BNO₃
badge Registry Numbers
MDL Number MFCD16660305
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a key intermediate for constructing complex molecules. Its boronate ester group enables efficient coupling with aryl or vinyl halides, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its cyclopropyl moiety can impart unique structural and electronic properties to the final products, enhancing their biological activity or stability. Researchers also employ it in the synthesis of bioactive compounds, including potential drug candidates, due to its versatility and reactivity in forming carbon-carbon bonds.

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

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N-Cyclopropyl-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetamide
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a key intermediate for constructing complex molecules. Its boronate ester group enables efficient coupling with aryl or vinyl halides, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its cyclopropyl moiety can impart unique structural and electronic properties to the final products, enhancing

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a key intermediate for constructing complex molecules. Its boronate ester group enables efficient coupling with aryl or vinyl halides, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its cyclopropyl moiety can impart unique structural and electronic properties to the final products, enhancing their biological activity or stability. Researchers also employ it in the synthesis of bioactive compounds, including potential drug candidates, due to its versatility and reactivity in forming carbon-carbon bonds.

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