(2S,4R)-4-Fluoropyrrolidine-2-carboxylic acid hydrochloride

97%

  • Product Code: 76145
  CAS:    60604-36-6
Molecular Weight: 169.58 g./mol Molecular Formula: C₅H₉ClFNO₂
EC Number: MDL Number: MFCD11053638
Melting Point: Boiling Point:
Density: Storage Condition: Room temperature, sealed, dry
Product Description: This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various bioactive molecules and drug candidates. Its unique stereochemistry and fluorine substitution make it valuable for designing compounds with enhanced metabolic stability and binding affinity. It is often employed in the development of protease inhibitors, particularly those targeting enzymes like dipeptidyl peptidase-4 (DPP-4), which are relevant in the treatment of type 2 diabetes. Additionally, its structural features are explored in the creation of peptidomimetics, which mimic natural peptides to modulate biological pathways. Its hydrochloride form ensures better solubility and handling in experimental settings, facilitating its use in both laboratory and industrial-scale applications.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days £27.89
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1.000 10-20 days £70.02
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5.000 10-20 days £238.56
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(2S,4R)-4-Fluoropyrrolidine-2-carboxylic acid hydrochloride
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various bioactive molecules and drug candidates. Its unique stereochemistry and fluorine substitution make it valuable for designing compounds with enhanced metabolic stability and binding affinity. It is often employed in the development of protease inhibitors, particularly those targeting enzymes like dipeptidyl peptidase-4 (DPP-4), which are relevant in the treatment of type 2 diabetes. Additionally, its structural features are explored in the creation of peptidomimetics, which mimic natural peptides to modulate biological pathways. Its hydrochloride form ensures better solubility and handling in experimental settings, facilitating its use in both laboratory and industrial-scale applications.
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