1-(pyridin-2-yl)-3-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)urea

95%

Reagent Code: #90037
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CAS Number 874301-59-4

science Other reagents with same CAS 874301-59-4

blur_circular Chemical Specifications

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Weight 339.19658 g/mol
Formula C₁₈H₂₂BN₃O₃
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions. Its boronate ester group makes it a valuable intermediate in Suzuki-Miyaura coupling, a widely used method for forming carbon-carbon bonds. This reaction is essential in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Additionally, the pyridine moiety can enhance the compound's ability to interact with biological targets, making it potentially useful in medicinal chemistry for drug discovery and development. Its structure also allows for further functionalization, enabling the creation of diverse derivatives for various research and industrial applications.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿5,391.00
inventory 250mg
10-20 days ฿21,582.00

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1-(pyridin-2-yl)-3-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)urea
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions. Its boronate ester group makes it a valuable intermediate in Suzuki-Miyaura coupling, a widely used method for forming carbon-carbon bonds. This reaction is essential in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Additionally, the pyridine moiety can enhance the compound's ability to interact with biological targets, making it potentially u

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions. Its boronate ester group makes it a valuable intermediate in Suzuki-Miyaura coupling, a widely used method for forming carbon-carbon bonds. This reaction is essential in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Additionally, the pyridine moiety can enhance the compound's ability to interact with biological targets, making it potentially useful in medicinal chemistry for drug discovery and development. Its structure also allows for further functionalization, enabling the creation of diverse derivatives for various research and industrial applications.

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