Methyl (2S,4R)-4-fluoroprolinate

95%

  • Product Code: 104152
  CAS:    126111-11-3
Molecular Weight: 147.15 g./mol Molecular Formula: C₆H₁₀FNO₂
EC Number: MDL Number: MFCD06796153
Melting Point: Boiling Point: 180.7 °C(Predicted)
Density: 1.15 g/cm3(Predicted) Storage Condition: room temperature
Product Description: This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its structure, featuring a fluorine atom and a prolinate backbone, makes it valuable for developing drugs with enhanced metabolic stability and bioavailability. It is often employed in the production of protease inhibitors, which are crucial in treating diseases such as hepatitis C and HIV. Additionally, its chiral centers allow for the creation of enantiomerically pure compounds, which are essential for ensuring the efficacy and safety of therapeutic agents. The compound’s unique properties also make it a candidate for research in medicinal chemistry, particularly in designing molecules with specific biological activities.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days £223.91
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0.250 10-20 days £375.56
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1.000 10-20 days £751.11
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Methyl (2S,4R)-4-fluoroprolinate
This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its structure, featuring a fluorine atom and a prolinate backbone, makes it valuable for developing drugs with enhanced metabolic stability and bioavailability. It is often employed in the production of protease inhibitors, which are crucial in treating diseases such as hepatitis C and HIV. Additionally, its chiral centers allow for the creation of enantiomerically pure compounds, which are essential for ensuring the efficacy and safety of therapeutic agents. The compound’s unique properties also make it a candidate for research in medicinal chemistry, particularly in designing molecules with specific biological activities.
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