(3S)-3-(2,2,2-Trifluoroethyl)pyrrolidinehydrochloride

98%

Reagent Code: #237725
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CAS Number 2639960-45-3

science Other reagents with same CAS 2639960-45-3

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Weight 189.61 g/mol
Formula C₆H₁₁ClF₃N
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Storage Room temperature

description Product Description

Used as a key chiral intermediate in the synthesis of biologically active pharmaceuticals, particularly in the development of protease inhibitors and antiviral agents. Its trifluoroethyl group enhances metabolic stability and membrane permeability, making it valuable in optimizing drug candidates. Commonly employed in medicinal chemistry for structure-activity relationship studies due to its rigid pyrrolidine scaffold and fluorinated side chain. Also utilized in the preparation of enzyme inhibitors where stereochemistry plays a critical role in activity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,680.00
inventory 250mg
10-20 days ฿14,310.00
inventory 1g
10-20 days ฿23,020.00
inventory 5g
10-20 days ฿84,790.00
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(3S)-3-(2,2,2-Trifluoroethyl)pyrrolidinehydrochloride
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Used as a key chiral intermediate in the synthesis of biologically active pharmaceuticals, particularly in the development of protease inhibitors and antiviral agents. Its trifluoroethyl group enhances metabolic stability and membrane permeability, making it valuable in optimizing drug candidates. Commonly employed in medicinal chemistry for structure-activity relationship studies due to its rigid pyrrolidine scaffold and fluorinated side chain. Also utilized in the preparation of enzyme inhibitors where

Used as a key chiral intermediate in the synthesis of biologically active pharmaceuticals, particularly in the development of protease inhibitors and antiviral agents. Its trifluoroethyl group enhances metabolic stability and membrane permeability, making it valuable in optimizing drug candidates. Commonly employed in medicinal chemistry for structure-activity relationship studies due to its rigid pyrrolidine scaffold and fluorinated side chain. Also utilized in the preparation of enzyme inhibitors where stereochemistry plays a critical role in activity.

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