tert-butyl 4-(5-(methoxycarbonyl)pyridin-2-yl)piperazine-1-carboxylate

98%

Reagent Code: #241766
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CAS Number 857284-21-0

science Other reagents with same CAS 857284-21-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 321.38 g/mol
Formula C₁₆H₂₃N₃O₄
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other bioactive molecules. Its piperazine core and pyridine functionality make it valuable for constructing drug candidates targeting neurological disorders, inflammation, and cancer. The tert-butyl carbamate (Boc) group allows for easy protection of amines during multi-step syntheses, while the methoxycarbonyl moiety can be hydrolyzed or transformed to introduce additional functional groups. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its favorable solubility and ability to modulate molecular polarity.

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inventory 1g
10-20 days ฿4,746.50

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tert-butyl 4-(5-(methoxycarbonyl)pyridin-2-yl)piperazine-1-carboxylate
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Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other bioactive molecules. Its piperazine core and pyridine functionality make it valuable for constructing drug candidates targeting neurological disorders, inflammation, and cancer. The tert-butyl carbamate (Boc) group allows for easy protection of amines during multi-step syntheses, while the methoxycarbonyl moiety can be hydrolyzed or transformed to introduce additional functional groups. Com

Used as an intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other bioactive molecules. Its piperazine core and pyridine functionality make it valuable for constructing drug candidates targeting neurological disorders, inflammation, and cancer. The tert-butyl carbamate (Boc) group allows for easy protection of amines during multi-step syntheses, while the methoxycarbonyl moiety can be hydrolyzed or transformed to introduce additional functional groups. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its favorable solubility and ability to modulate molecular polarity.

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