(9H-fluoren-9-yl)methyl3-oxopiperidine-1-carboxylate

98%

Reagent Code: #196219
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CAS Number 672310-11-1

science Other reagents with same CAS 672310-11-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 321.37 g/mol
Formula C₂₀H₁₉NO₃
badge Registry Numbers
MDL Number MFCD03001740
thermostat Physical Properties
Melting Point 90-96 °C
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the development of pharmaceuticals. It serves as a building block for creating complex nitrogen-containing heterocycles, which are common in bioactive molecules. Its structure allows for selective modifications, making it valuable in medicinal chemistry for drug discovery. Commonly employed in the synthesis of protease inhibitors and central nervous system agents due to the stability and reactivity of the piperidine ring protected by the fluorenyl group. Also utilized in solid-phase peptide synthesis as a protecting group strategy when modified appropriately.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿5,060.00
5g
10-20 days ฿15,350.00
(9H-fluoren-9-yl)methyl3-oxopiperidine-1-carboxylate
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Used primarily as an intermediate in organic synthesis, especially in the development of pharmaceuticals. It serves as a building block for creating complex nitrogen-containing heterocycles, which are common in bioactive molecules. Its structure allows for selective modifications, making it valuable in medicinal chemistry for drug discovery. Commonly employed in the synthesis of protease inhibitors and central nervous system agents due to the stability and reactivity of the piperidine ring protected by t

Used primarily as an intermediate in organic synthesis, especially in the development of pharmaceuticals. It serves as a building block for creating complex nitrogen-containing heterocycles, which are common in bioactive molecules. Its structure allows for selective modifications, making it valuable in medicinal chemistry for drug discovery. Commonly employed in the synthesis of protease inhibitors and central nervous system agents due to the stability and reactivity of the piperidine ring protected by the fluorenyl group. Also utilized in solid-phase peptide synthesis as a protecting group strategy when modified appropriately.

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