(S)-tert-Butyl 2-carbamothioylpyrrolidine-1-carboxylate

≥98%

Reagent Code: #235064
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CAS Number 101410-18-8

science Other reagents with same CAS 101410-18-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 230.33 g/mol
Formula C₁₀H₁₈N₂O₂S
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its protected thioamide functionality allows for selective transformations in multi-step organic syntheses. Commonly employed in medicinal chemistry for constructing peptidomimetic structures due to its ability to mimic peptide bonds while enhancing metabolic stability. Also utilized in asymmetric synthesis to introduce stereochemical control in drug candidates.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿253.00
inventory 250mg
10-20 days ฿346.50
inventory 1g
10-20 days ฿1,199.00
inventory 5g
10-20 days ฿10,830.00
(S)-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 and other bioactive molecules. Its protected thioamide functionality allows for selective transformations in multi-step organic syntheses. Commonly employed in medicinal chemistry for constructing peptidomimetic structures due to its ability to mimic peptide bonds while enhancing metabolic stability. Also utilized in asymmetric synthesis to introduce stereochemical control in drug can

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its protected thioamide functionality allows for selective transformations in multi-step organic syntheses. Commonly employed in medicinal chemistry for constructing peptidomimetic structures due to its ability to mimic peptide bonds while enhancing metabolic stability. Also utilized in asymmetric synthesis to introduce stereochemical control in drug candidates.

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