(2S,4S)-1-tert-Butyl 2-methyl 4-aminopiperidine-1,2-dicarboxylate

98%

Reagent Code: #233418
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CAS Number 254882-09-2

science Other reagents with same CAS 254882-09-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 258.31 g/mol
Formula C₁₂H₂₂N₂O₄
badge Registry Numbers
MDL Number MFCD18071999
inventory_2 Storage & Handling
Storage 2-8°C, away from light, dry

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of protease inhibitors and other bioactive molecules. Its protected amine and functionalized piperidine backbone make it valuable in medicinal chemistry for constructing complex, stereochemically defined drug candidates. Commonly employed in the preparation of antiviral and anticancer compounds where precise stereochemistry is critical for biological activity. The tert-butyl and methyl ester groups allow for selective deprotection and further derivatization in multi-step synthetic routes.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿12,510.00
inventory 100mg
10-20 days ฿21,320.00
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(2S,4S)-1-tert-Butyl 2-methyl 4-aminopiperidine-1,2-dicarboxylate
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Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of protease inhibitors and other bioactive molecules. Its protected amine and functionalized piperidine backbone make it valuable in medicinal chemistry for constructing complex, stereochemically defined drug candidates. Commonly employed in the preparation of antiviral and anticancer compounds where precise stereochemistry is critical for biological activity. The tert-butyl and methyl ester group

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of protease inhibitors and other bioactive molecules. Its protected amine and functionalized piperidine backbone make it valuable in medicinal chemistry for constructing complex, stereochemically defined drug candidates. Commonly employed in the preparation of antiviral and anticancer compounds where precise stereochemistry is critical for biological activity. The tert-butyl and methyl ester groups allow for selective deprotection and further derivatization in multi-step synthetic routes.

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