(3S,4R)-Benzyl 4-((tert-butoxycarbonyl)amino)-3-fluoropiperidine-1-carboxylate

95%

Reagent Code: #233443
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CAS Number 1932010-74-6

science Other reagents with same CAS 1932010-74-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 352.4 g/mol
Formula C₁₈H₂₅FN₂O₄
badge Registry Numbers
MDL Number MFCD28010159
thermostat Physical Properties
Boiling Point 478.7±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.19±0.1 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of protease inhibitors and antiviral drugs. Its chiral structure with defined stereochemistry makes it valuable for constructing complex molecules where stereo-selectivity is critical. The presence of amine protecting groups (Boc and Cbz) allows for stepwise coupling and deprotection strategies in multi-step organic syntheses. Commonly employed in medicinal chemistry for building blocks in drug discovery programs targeting hepatitis C virus (HCV) and other viral diseases.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿17,600.00
inventory 250mg
10-20 days ฿29,920.00
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(3S,4R)-Benzyl 4-((tert-butoxycarbonyl)amino)-3-fluoropiperidine-1-carboxylate
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of protease inhibitors and antiviral drugs. Its chiral structure with defined stereochemistry makes it valuable for constructing complex molecules where stereo-selectivity is critical. The presence of amine protecting groups (Boc and Cbz) allows for stepwise coupling and deprotection strategies in multi-step organic syntheses. Commonly employed in medicinal chemistry for building blocks in drug discovery

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of protease inhibitors and antiviral drugs. Its chiral structure with defined stereochemistry makes it valuable for constructing complex molecules where stereo-selectivity is critical. The presence of amine protecting groups (Boc and Cbz) allows for stepwise coupling and deprotection strategies in multi-step organic syntheses. Commonly employed in medicinal chemistry for building blocks in drug discovery programs targeting hepatitis C virus (HCV) and other viral diseases.

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