5-Chloro-3-((trimethylsilyl)-ethynyl)pyrazin-2-amine

≥95%

Reagent Code: #124372
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CAS Number 1244776-64-4

science Other reagents with same CAS 1244776-64-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 225.75 g/mol
Formula C₉H₁₂ClN₃Si
badge Registry Numbers
MDL Number MFCD26517225
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, inert gas

description Product Description

This compound is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of complex molecules, particularly in the construction of pyrazine-based structures. Its trimethylsilyl-ethynyl group makes it valuable in cross-coupling reactions, enabling the formation of carbon-carbon bonds, which are crucial in drug discovery and material science. Additionally, its chloro and amine functional groups allow for further derivatization, making it versatile in designing compounds with potential biological activity, such as antimicrobial or anticancer agents. Its application is often seen in medicinal chemistry for synthesizing novel therapeutic candidates.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿8,055.00
inventory 1g
10-20 days ฿20,133.00
inventory 100mg
10-20 days ฿5,391.00
5-Chloro-3-((trimethylsilyl)-ethynyl)pyrazin-2-amine
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This compound is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of complex molecules, particularly in the construction of pyrazine-based structures. Its trimethylsilyl-ethynyl group makes it valuable in cross-coupling reactions, enabling the formation of carbon-carbon bonds, which are crucial in drug discovery and material science. Additionally, its chloro and amine functional groups allow for further derivatization, making it versa

This compound is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of complex molecules, particularly in the construction of pyrazine-based structures. Its trimethylsilyl-ethynyl group makes it valuable in cross-coupling reactions, enabling the formation of carbon-carbon bonds, which are crucial in drug discovery and material science. Additionally, its chloro and amine functional groups allow for further derivatization, making it versatile in designing compounds with potential biological activity, such as antimicrobial or anticancer agents. Its application is often seen in medicinal chemistry for synthesizing novel therapeutic candidates.

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