tert-Butyl ((3R,5S)-5-(hydroxymethyl)pyrrolidin-3-yl)carbamate

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Reagent Code: #152354
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CAS Number 1264243-41-5

science Other reagents with same CAS 1264243-41-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 216.28 g/mol
Formula C₁₀H₂₀N₂O₃
badge Registry Numbers
MDL Number MFCD08704528
thermostat Physical Properties
Boiling Point 351.4±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.11±0.1 g/cm3(Predicted)
Storage Room temperature, avoid light

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of antiviral and antidiabetic drugs. Its protected amine and hydroxyl functional groups allow for selective chemical modifications, making it valuable in constructing complex bioactive molecules. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its stereochemical purity and ability to enhance drug potency and selectivity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,150.00
inventory 250mg
10-20 days ฿8,530.00
inventory 1g
10-20 days ฿27,520.00

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tert-Butyl ((3R,5S)-5-(hydroxymethyl)pyrrolidin-3-yl)carbamate
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Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of antiviral and antidiabetic drugs. Its protected amine and hydroxyl functional groups allow for selective chemical modifications, making it valuable in constructing complex bioactive molecules. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its stereochemical purity and ability to enhance drug potency and selectivity.

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of antiviral and antidiabetic drugs. Its protected amine and hydroxyl functional groups allow for selective chemical modifications, making it valuable in constructing complex bioactive molecules. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its stereochemical purity and ability to enhance drug potency and selectivity.

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