(R)-Tert-Butyl 2-Carbamothioylpyrrolidine-1-Carboxylate

95%

Reagent Code: #230927
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CAS Number 117175-41-4

science Other reagents with same CAS 117175-41-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 230.33 g/mol
Formula C₁₀H₁₈N₂O₂S
badge Registry Numbers
MDL Number MFCD06738836
thermostat Physical Properties
Melting Point 200-201 °C
Boiling Point 339.5±52.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.191±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors. Its structure supports the formation of thioamide derivatives, which are valuable in drug design for enhancing metabolic stability and binding affinity. Commonly employed in asymmetric synthesis due to the presence of a stereogenic center, enabling the production of enantiomerically pure compounds. Also utilized in the preparation of enzyme inhibitors where the pyrrolidine ring acts as a proline mimic in peptide-based therapeutics.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,240.00
inventory 250mg
10-20 days ฿6,080.00
inventory 1g
10-20 days ฿12,170.00
(R)-Tert-Butyl 2-Carbamothioylpyrrolidine-1-Carboxylate
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Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors. Its structure supports the formation of thioamide derivatives, which are valuable in drug design for enhancing metabolic stability and binding affinity. Commonly employed in asymmetric synthesis due to the presence of a stereogenic center, enabling the production of enantiomerically pure compounds. Also utilized in the preparation of enzyme inhibitors where the pyrrolidine ring acts

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors. Its structure supports the formation of thioamide derivatives, which are valuable in drug design for enhancing metabolic stability and binding affinity. Commonly employed in asymmetric synthesis due to the presence of a stereogenic center, enabling the production of enantiomerically pure compounds. Also utilized in the preparation of enzyme inhibitors where the pyrrolidine ring acts as a proline mimic in peptide-based therapeutics.

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