(2S,4S)-1-(tert-butoxycarbonyl)-2-methylpiperidine-4-carboxylicacid

98%

Reagent Code: #237658
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CAS Number 1820583-83-2

science Other reagents with same CAS 1820583-83-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 243.30 g/mol
Formula C₁₂H₂₁NO₄
badge Registry Numbers
MDL Number MFCD28139503
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other biologically active molecules. Its (2S,4S) stereochemistry allows for selective interactions in drug design, enhancing potency and specificity. Commonly employed in medicinal chemistry for constructing complex cyclic frameworks found in antiviral and anticancer agents. The Boc-protected amine and carboxylic acid functionalities enable stepwise coupling reactions, making it valuable in solid-phase and solution-phase peptide-like synthesis.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿17,380.00
inventory 500mg
10-20 days ฿48,750.00
inventory 1g
10-20 days ฿85,320.00
inventory 250mg
10-20 days ฿27,800.00
(2S,4S)-1-(tert-butoxycarbonyl)-2-methylpiperidine-4-carboxylicacid
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Used as a key chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other biologically active molecules. Its (2S,4S) stereochemistry allows for selective interactions in drug design, enhancing potency and specificity. Commonly employed in medicinal chemistry for constructing complex cyclic frameworks found in antiviral and anticancer agents. The Boc-protected amine and carboxylic acid functionalities enable stepwise coupling reactions

Used as a key chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other biologically active molecules. Its (2S,4S) stereochemistry allows for selective interactions in drug design, enhancing potency and specificity. Commonly employed in medicinal chemistry for constructing complex cyclic frameworks found in antiviral and anticancer agents. The Boc-protected amine and carboxylic acid functionalities enable stepwise coupling reactions, making it valuable in solid-phase and solution-phase peptide-like synthesis.

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