1-Boc-4-Cbz-aminoazepane

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Reagent Code: #148157
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CAS Number 878630-96-7

science Other reagents with same CAS 878630-96-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 348.44 g/mol
Formula C₁₉H₂₈N₂O₄
badge Registry Numbers
MDL Number MFCD18207774
thermostat Physical Properties
Boiling Point 484.9±44.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in inert gas

description Product Description

Used in pharmaceutical synthesis as a protected intermediate for developing bioactive molecules, particularly in the construction of nitrogen-containing heterocycles. The Boc and Cbz protecting groups allow selective manipulation of the amine functionality during multi-step reactions, making it valuable in the preparation of drug candidates targeting central nervous system disorders. Its seven-membered ring structure supports conformational studies in medicinal chemistry, aiding the design of receptor-targeted compounds. Commonly employed in solid-phase and solution-phase peptide-like synthesis where controlled deprotection and coupling are required.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿5,080.00
inventory 1g
10-20 days ฿11,670.00
inventory 5g
10-20 days ฿35,750.00

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1-Boc-4-Cbz-aminoazepane
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Used in pharmaceutical synthesis as a protected intermediate for developing bioactive molecules, particularly in the construction of nitrogen-containing heterocycles. The Boc and Cbz protecting groups allow selective manipulation of the amine functionality during multi-step reactions, making it valuable in the preparation of drug candidates targeting central nervous system disorders. Its seven-membered ring structure supports conformational studies in medicinal chemistry, aiding the design of receptor-ta

Used in pharmaceutical synthesis as a protected intermediate for developing bioactive molecules, particularly in the construction of nitrogen-containing heterocycles. The Boc and Cbz protecting groups allow selective manipulation of the amine functionality during multi-step reactions, making it valuable in the preparation of drug candidates targeting central nervous system disorders. Its seven-membered ring structure supports conformational studies in medicinal chemistry, aiding the design of receptor-targeted compounds. Commonly employed in solid-phase and solution-phase peptide-like synthesis where controlled deprotection and coupling are required.

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