1-((tert-Butoxycarbonyl)amino)-3,3-difluorocyclopentanecarboxylic acid

98%

  • Product Code: 39089
  CAS:    1936649-94-3
Molecular Weight: 265.25 g./mol Molecular Formula: C₁₁H₁₇F₂NO₄
EC Number: MDL Number: MFCD28501988
Melting Point: Boiling Point:
Density: Storage Condition: room temperature
Product Description: This compound is primarily utilized in the pharmaceutical and organic synthesis industries as a key intermediate in the production of more complex molecules. Its structure, featuring both a tert-butoxycarbonyl (Boc) protecting group and a difluorinated cyclopentane ring, makes it valuable for constructing peptides and small molecules with enhanced stability and bioavailability. The Boc group can be selectively removed under mild acidic conditions, allowing for further functionalization of the molecule. Additionally, the presence of fluorine atoms can improve metabolic stability and binding affinity in drug candidates, making it particularly useful in the development of therapeutics targeting enzymes or receptors. Its application is also seen in the synthesis of bioactive compounds for research purposes, aiding in the study of structure-activity relationships.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days $636.51
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1-((tert-Butoxycarbonyl)amino)-3,3-difluorocyclopentanecarboxylic acid
This compound is primarily utilized in the pharmaceutical and organic synthesis industries as a key intermediate in the production of more complex molecules. Its structure, featuring both a tert-butoxycarbonyl (Boc) protecting group and a difluorinated cyclopentane ring, makes it valuable for constructing peptides and small molecules with enhanced stability and bioavailability. The Boc group can be selectively removed under mild acidic conditions, allowing for further functionalization of the molecule. Additionally, the presence of fluorine atoms can improve metabolic stability and binding affinity in drug candidates, making it particularly useful in the development of therapeutics targeting enzymes or receptors. Its application is also seen in the synthesis of bioactive compounds for research purposes, aiding in the study of structure-activity relationships.
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