trans-1-(tert-butoxycarbonyl)-4-(4-fluorophenyl)pyrrolidine-3-carboxylic acid

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Reagent Code: #242141
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CAS Number 1218764-11-4

science Other reagents with same CAS 1218764-11-4

blur_circular Chemical Specifications

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Weight 309.34 g/mol
Formula C₁₆H₂₀FNO₄
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of protease inhibitors and other biologically active molecules. Its structure supports the formation of peptidomimetic compounds, making it valuable in drug discovery for metabolic and neurological disorders. The fluorophenyl and Boc-protected pyrrolidine moieties enhance binding selectivity and stability in target enzymes. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its conformational rigidity and functional group compatibility in coupling reactions.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿3,200.00
inventory 250mg
10-20 days ฿9,510.00
inventory 1g
10-20 days ฿23,910.00

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trans-1-(tert-butoxycarbonyl)-4-(4-fluorophenyl)pyrrolidine-3-carboxylic acid
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of protease inhibitors and other biologically active molecules. Its structure supports the formation of peptidomimetic compounds, making it valuable in drug discovery for metabolic and neurological disorders. The fluorophenyl and Boc-protected pyrrolidine moieties enhance binding selectivity and stability in target enzymes. Commonly employed in medicinal chemistry for structure-activity relationship (SAR

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of protease inhibitors and other biologically active molecules. Its structure supports the formation of peptidomimetic compounds, making it valuable in drug discovery for metabolic and neurological disorders. The fluorophenyl and Boc-protected pyrrolidine moieties enhance binding selectivity and stability in target enzymes. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its conformational rigidity and functional group compatibility in coupling reactions.

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