Benzyl (R)-2-formylpyrrolidine-1-carboxylate

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Reagent Code: #229227
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CAS Number 143393-11-7

science Other reagents with same CAS 143393-11-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.26 g/mol
Formula C₁₃H₁₅NO₃
badge Registry Numbers
MDL Number MFCD09842196
thermostat Physical Properties
Boiling Point 369.6±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.263±0.06 g/cm3(Predicted)
Storage -20°C, Sealed, Inert Gas

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of protease inhibitors and other bioactive molecules. Its protected aldehyde functionality allows for selective reactions in multi-step organic syntheses. Commonly employed in the development of antiviral and anticancer agents due to its ability to mimic peptide structures and enhance metabolic stability. Also utilized in asymmetric synthesis to introduce stereochemical control in drug candidates.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,240.00
inventory 250mg
10-20 days ฿14,000.00

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Benzyl (R)-2-formylpyrrolidine-1-carboxylate
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Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of protease inhibitors and other bioactive molecules. Its protected aldehyde functionality allows for selective reactions in multi-step organic syntheses. Commonly employed in the development of antiviral and anticancer agents due to its ability to mimic peptide structures and enhance metabolic stability. Also utilized in asymmetric synthesis to introduce stereochemical control in drug candidates.

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of protease inhibitors and other bioactive molecules. Its protected aldehyde functionality allows for selective reactions in multi-step organic syntheses. Commonly employed in the development of antiviral and anticancer agents due to its ability to mimic peptide structures and enhance metabolic stability. Also utilized in asymmetric synthesis to introduce stereochemical control in drug candidates.

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