tert-Butyl 3-(pyrazin-2-yl)azetidine-1-carboxylate

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Reagent Code: #44518
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CAS Number 1146085-63-3

science Other reagents with same CAS 1146085-63-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 235.2823 g/mol
Formula C₁₂H₁₇N₃O₂
badge Registry Numbers
MDL Number MFCD20528746
inventory_2 Storage & Handling
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description Product Description

This chemical is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of biologically active compounds. Its structure, featuring a pyrazine ring and an azetidine moiety, makes it valuable for designing molecules with potential therapeutic applications, particularly in the fields of oncology and central nervous system disorders. It is often employed in medicinal chemistry to explore structure-activity relationships (SAR) and optimize drug candidates for improved efficacy and selectivity. Additionally, its tert-butyl carboxylate group serves as a protective group during synthetic processes, enabling precise modifications to the molecule.

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inventory 100mg
10-20 days ฿3,645.00

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tert-Butyl 3-(pyrazin-2-yl)azetidine-1-carboxylate
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This chemical is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of biologically active compounds. Its structure, featuring a pyrazine ring and an azetidine moiety, makes it valuable for designing molecules with potential therapeutic applications, particularly in the fields of oncology and central nervous system disorders. It is often employed in medicinal chemistry to explore structure-activity relationships (SAR) and optimize drug candidates for improve
This chemical is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of biologically active compounds. Its structure, featuring a pyrazine ring and an azetidine moiety, makes it valuable for designing molecules with potential therapeutic applications, particularly in the fields of oncology and central nervous system disorders. It is often employed in medicinal chemistry to explore structure-activity relationships (SAR) and optimize drug candidates for improved efficacy and selectivity. Additionally, its tert-butyl carboxylate group serves as a protective group during synthetic processes, enabling precise modifications to the molecule.
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