(2S,4R)-4-(4-Fluorobenzyl)pyrrolidine-2-carboxylic acid

95%

Reagent Code: #233227
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CAS Number 1049977-93-6

science Other reagents with same CAS 1049977-93-6

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scatter_plot Molecular Information
Weight 223.24 g/mol
Formula C₁₂H₁₄FNO₂
badge Registry Numbers
MDL Number MFCD17215176
inventory_2 Storage & Handling
Storage 2-8°C, away from light, dry

description Product Description

Used as a key intermediate in the synthesis of antidiabetic drugs, particularly in the production of DPP-4 inhibitors like vildagliptin and saxagliptin. Its chiral structure enables selective interaction with biological targets, enhancing drug efficacy and reducing side effects. Commonly employed in pharmaceutical research for developing oral hypoglycemic agents. Also utilized in asymmetric synthesis due to its stereochemical purity, supporting the development of enantiomerically pure therapeutics.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,690.00
inventory 250mg
10-20 days ฿18,160.00

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(2S,4R)-4-(4-Fluorobenzyl)pyrrolidine-2-carboxylic acid
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Used as a key intermediate in the synthesis of antidiabetic drugs, particularly in the production of DPP-4 inhibitors like vildagliptin and saxagliptin. Its chiral structure enables selective interaction with biological targets, enhancing drug efficacy and reducing side effects. Commonly employed in pharmaceutical research for developing oral hypoglycemic agents. Also utilized in asymmetric synthesis due to its stereochemical purity, supporting the development of enantiomerically pure therapeutics.
Used as a key intermediate in the synthesis of antidiabetic drugs, particularly in the production of DPP-4 inhibitors like vildagliptin and saxagliptin. Its chiral structure enables selective interaction with biological targets, enhancing drug efficacy and reducing side effects. Commonly employed in pharmaceutical research for developing oral hypoglycemic agents. Also utilized in asymmetric synthesis due to its stereochemical purity, supporting the development of enantiomerically pure therapeutics.
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