5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidin-4-amine

95%

Reagent Code: #90797
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CAS Number 2223044-20-8

science Other reagents with same CAS 2223044-20-8

blur_circular Chemical Specifications

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Weight 239.07922 g/mol
Formula C₁₀H₁₈BN₃O₃
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are essential for constructing carbon-carbon bonds in pharmaceuticals and materials science. Its boronate ester group makes it a valuable intermediate for introducing the pyrimidin-4-amine moiety into complex molecules, which is crucial in developing drugs targeting cancer, inflammation, and infectious diseases. Additionally, it serves as a building block in the synthesis of agrochemicals and organic electronic materials, contributing to advancements in crop protection and optoelectronic devices. Its stability and reactivity under mild conditions make it a preferred choice for chemists in various research and industrial applications.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿9,612.00
inventory 25mg
10-20 days ฿21,600.00

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5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidin-4-amine
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This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are essential for constructing carbon-carbon bonds in pharmaceuticals and materials science. Its boronate ester group makes it a valuable intermediate for introducing the pyrimidin-4-amine moiety into complex molecules, which is crucial in developing drugs targeting cancer, inflammation, and infectious diseases. Additionally, it serves as a building block in the synthesis of agrochemicals and

This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are essential for constructing carbon-carbon bonds in pharmaceuticals and materials science. Its boronate ester group makes it a valuable intermediate for introducing the pyrimidin-4-amine moiety into complex molecules, which is crucial in developing drugs targeting cancer, inflammation, and infectious diseases. Additionally, it serves as a building block in the synthesis of agrochemicals and organic electronic materials, contributing to advancements in crop protection and optoelectronic devices. Its stability and reactivity under mild conditions make it a preferred choice for chemists in various research and industrial applications.

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