(S)-tert-Butyl 2-(1H-imidazol-2-yl)pyrrolidine-1-carboxylate

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Reagent Code: #236154
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CAS Number 1007882-58-7

science Other reagents with same CAS 1007882-58-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 237.3 g/mol
Formula C₁₂H₁₉N₃O₂
badge Registry Numbers
MDL Number MFCD16660093
thermostat Physical Properties
Boiling Point 422.6±38.0 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of antiviral and antifungal drugs. Its imidazole-containing pyrrolidine structure enables effective binding to biological targets, making it valuable in medicinal chemistry for designing enzyme inhibitors. Commonly employed in asymmetric synthesis to introduce stereochemical control, it helps optimize the potency and selectivity of active pharmaceutical ingredients. Also utilized in research settings for constructing peptidomimetic compounds and probing structure-activity relationships in drug candidates.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,730.00
inventory 5g
10-20 days ฿34,760.00
inventory 1g
10-20 days ฿8,290.00
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(S)-tert-Butyl 2-(1H-imidazol-2-yl)pyrrolidine-1-carboxylate
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Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of antiviral and antifungal drugs. Its imidazole-containing pyrrolidine structure enables effective binding to biological targets, making it valuable in medicinal chemistry for designing enzyme inhibitors. Commonly employed in asymmetric synthesis to introduce stereochemical control, it helps optimize the potency and selectivity of active pharmaceutical ingredients. Also utilized in research setti

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of antiviral and antifungal drugs. Its imidazole-containing pyrrolidine structure enables effective binding to biological targets, making it valuable in medicinal chemistry for designing enzyme inhibitors. Commonly employed in asymmetric synthesis to introduce stereochemical control, it helps optimize the potency and selectivity of active pharmaceutical ingredients. Also utilized in research settings for constructing peptidomimetic compounds and probing structure-activity relationships in drug candidates.

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