(2S,4S)-1-(tert-Butoxycarbonyl)-4-(methoxymethyl)pyrrolidine-2-carboxylic acid

95%

Reagent Code: #234962
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CAS Number 1378388-16-9

science Other reagents with same CAS 1378388-16-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 259.3 g/mol
Formula C₁₂H₂₁NO₅
thermostat Physical Properties
Boiling Point 371.2±27.0°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 biologically active compounds. Its protected amine and carboxylic acid functionalities make it suitable for peptide coupling and solid-phase synthesis. The pyrrolidine ring with defined stereochemistry supports conformational control in drug design, enhancing selectivity and potency. Commonly employed in medicinal chemistry for structure-activity relationship studies and as an intermediate in the preparation of enzyme inhibitors targeting viral or metabolic diseases.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,080.00
inventory 10g
10-20 days ฿2,150.00
(2S,4S)-1-(tert-Butoxycarbonyl)-4-(methoxymethyl)pyrrolidine-2-carboxylic acid
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other biologically active compounds. Its protected amine and carboxylic acid functionalities make it suitable for peptide coupling and solid-phase synthesis. The pyrrolidine ring with defined stereochemistry supports conformational control in drug design, enhancing selectivity and potency. Commonly employed in medicinal chemistry for structure-activity relationship studies and a

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other biologically active compounds. Its protected amine and carboxylic acid functionalities make it suitable for peptide coupling and solid-phase synthesis. The pyrrolidine ring with defined stereochemistry supports conformational control in drug design, enhancing selectivity and potency. Commonly employed in medicinal chemistry for structure-activity relationship studies and as an intermediate in the preparation of enzyme inhibitors targeting viral or metabolic diseases.

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