(3R,4R)-rel-Benzyl 4-((tert-butoxycarbonyl)amino)-3-hydroxypiperidine-1-carboxylate

97%

Reagent Code: #230815
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CAS Number 724787-52-4

science Other reagents with same CAS 724787-52-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 350.41 g/mol
Formula C₁₈H₂₆N₂O₅
badge Registry Numbers
MDL Number MFCD16036056
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Widely used in pharmaceutical synthesis, this compound serves as a key chiral intermediate in the production of biologically active molecules, particularly protease inhibitors. Its protected functional groups and defined stereochemistry make it valuable for constructing complex drug scaffolds, especially in antiviral and anticancer agents. The hydroxyl and amine groups allow for selective modifications, enabling stepwise assembly of target molecules in multi-step organic syntheses. It is especially favored in solid-phase and solution-phase peptide-like synthesis due to compatibility with standard protecting group strategies.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿1,350.00
1g
10-20 days ฿5,370.00
5g
10-20 days ฿26,770.00
(3R,4R)-rel-Benzyl 4-((tert-butoxycarbonyl)amino)-3-hydroxypiperidine-1-carboxylate
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Widely used in pharmaceutical synthesis, this compound serves as a key chiral intermediate in the production of biologically active molecules, particularly protease inhibitors. Its protected functional groups and defined stereochemistry make it valuable for constructing complex drug scaffolds, especially in antiviral and anticancer agents. The hydroxyl and amine groups allow for selective modifications, enabling stepwise assembly of target molecules in multi-step organic syntheses. It is especially favor

Widely used in pharmaceutical synthesis, this compound serves as a key chiral intermediate in the production of biologically active molecules, particularly protease inhibitors. Its protected functional groups and defined stereochemistry make it valuable for constructing complex drug scaffolds, especially in antiviral and anticancer agents. The hydroxyl and amine groups allow for selective modifications, enabling stepwise assembly of target molecules in multi-step organic syntheses. It is especially favored in solid-phase and solution-phase peptide-like synthesis due to compatibility with standard protecting group strategies.

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