(S)-tert-Butyl 3-mercaptopyrrolidine-1-carboxylate

95%

Reagent Code: #235107
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CAS Number 156371-85-6

science Other reagents with same CAS 156371-85-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 203.3 g/mol
Formula C₉H₁₇NO₂S
thermostat Physical Properties
Boiling Point 275.1±33.0°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its free thiol and protected amine (Boc) functionalities allow selective reactions at the thiol group and deprotection for coupling, making it valuable in peptide mimetics and drug design. Commonly employed in asymmetric synthesis to introduce stereochemical control. Also utilized in the preparation of cysteine analogs and in medicinal chemistry for constructing heterocyclic compounds with biological activity.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿291.50
inventory 250mg
10-20 days ฿610.50
inventory 1g
10-20 days ฿4,370.00
(S)-tert-Butyl 3-mercaptopyrrolidine-1-carboxylate
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its free thiol and protected amine (Boc) functionalities allow selective reactions at the thiol group and deprotection for coupling, making it valuable in peptide mimetics and drug design. Commonly employed in asymmetric synthesis to introduce stereochemical control. Also utilized in the preparation of cysteine analogs and in medicinal chemistry for co

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its free thiol and protected amine (Boc) functionalities allow selective reactions at the thiol group and deprotection for coupling, making it valuable in peptide mimetics and drug design. Commonly employed in asymmetric synthesis to introduce stereochemical control. Also utilized in the preparation of cysteine analogs and in medicinal chemistry for constructing heterocyclic compounds with biological activity.

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