1-Cbz-3,4-dihydro-2H-pyridine

95%

Reagent Code: #162660
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CAS Number 68471-58-9

science Other reagents with same CAS 68471-58-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.26 g/mol
Formula C₁₃H₁₅NO₂
badge Registry Numbers
MDL Number MFCD10566328
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive molecules. Its structure allows for selective functionalization at nitrogen and carbon positions, making it valuable in constructing nitrogen-containing heterocycles. Commonly employed in the development of protease inhibitors and central nervous system agents. The Cbz-protected dihydropyridine scaffold is also utilized in medicinal chemistry for building blocks in drug discovery, especially in routes requiring mild deprotection conditions.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,280.00
inventory 1g
10-20 days ฿9,260.00

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1-Cbz-3,4-dihydro-2H-pyridine
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive molecules. Its structure allows for selective functionalization at nitrogen and carbon positions, making it valuable in constructing nitrogen-containing heterocycles. Commonly employed in the development of protease inhibitors and central nervous system agents. The Cbz-protected dihydropyridine scaffold is also utilized in medicinal chemistry for building blocks in drug discovery, especially in

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive molecules. Its structure allows for selective functionalization at nitrogen and carbon positions, making it valuable in constructing nitrogen-containing heterocycles. Commonly employed in the development of protease inhibitors and central nervous system agents. The Cbz-protected dihydropyridine scaffold is also utilized in medicinal chemistry for building blocks in drug discovery, especially in routes requiring mild deprotection conditions.

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