(2S,4S)-1-[(tert-butoxy)carbonyl]-4-(trifluoromethyl)pyrrolidine-2-carboxylic acid

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Reagent Code: #237321
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CAS Number 470482-41-8

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Widely used in pharmaceutical synthesis, this compound serves as a chiral building block for the preparation of biologically active molecules. Its rigid pyrrolidine backbone and trifluoromethyl group enhance metabolic stability and binding selectivity in drug candidates. It is particularly valuable in the development of protease inhibitors and other enzyme-targeted therapies. The Boc-protected amine allows for straightforward deprotection and coupling in peptide-like synthesis, making it suitable for use in solid-phase and solution-phase applications. Its stereochemistry enables precise control over 3D structure, which is critical in optimizing potency and reducing off-target effects in medicinal chemistry programs.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,560.00
inventory 250mg
10-20 days ฿5,180.00
inventory 1g
10-20 days ฿20,660.00
inventory 5g
10-20 days ฿89,810.00
(2S,4S)-1-[(tert-butoxy)carbonyl]-4-(trifluoromethyl)pyrrolidine-2-carboxylic acid
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Widely used in pharmaceutical synthesis, this compound serves as a chiral building block for the preparation of biologically active molecules. Its rigid pyrrolidine backbone and trifluoromethyl group enhance metabolic stability and binding selectivity in drug candidates. It is particularly valuable in the development of protease inhibitors and other enzyme-targeted therapies. The Boc-protected amine allows for straightforward deprotection and coupling in peptide-like synthesis, making it suitable for use

Widely used in pharmaceutical synthesis, this compound serves as a chiral building block for the preparation of biologically active molecules. Its rigid pyrrolidine backbone and trifluoromethyl group enhance metabolic stability and binding selectivity in drug candidates. It is particularly valuable in the development of protease inhibitors and other enzyme-targeted therapies. The Boc-protected amine allows for straightforward deprotection and coupling in peptide-like synthesis, making it suitable for use in solid-phase and solution-phase applications. Its stereochemistry enables precise control over 3D structure, which is critical in optimizing potency and reducing off-target effects in medicinal chemistry programs.

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