(R)-BoroLeu-()-Pinanediol trifluoroacetate

98%

  • Product Code: 71341
  Alias:    (R)-1-Amino-3-methylbutyl borate pinanediol trifluoroacetate
  CAS:    179324-87-9
Molecular Weight: 379.22 g./mol Molecular Formula: C₁₇H₂₉BF₃NO₄
EC Number: MDL Number: MFCD10566030
Melting Point: Boiling Point:
Density: Storage Condition: 2-8°C, inert gas
Product Description: (R)-BoroLeu-()-Pinanediol trifluoroacetate is primarily utilized in the field of organic synthesis, particularly in peptide chemistry. It serves as a key reagent for the protection of amino groups during peptide bond formation, ensuring selective reactions and high yields. Its application extends to the synthesis of complex peptides and proteins, where precise control over amino acid coupling is essential. Additionally, it is employed in the development of boron-based drugs, leveraging its unique properties to enhance drug stability and bioavailability. In medicinal chemistry, it plays a role in creating targeted therapies, especially for conditions like cancer and infectious diseases, by facilitating the incorporation of boron into biologically active molecules. Its chiral nature also makes it valuable in asymmetric synthesis, enabling the production of enantiomerically pure compounds for pharmaceutical applications.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days £14.47
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1.000 10-20 days £51.57
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5.000 10-20 days £183.65
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(R)-BoroLeu-()-Pinanediol trifluoroacetate
(R)-BoroLeu-()-Pinanediol trifluoroacetate is primarily utilized in the field of organic synthesis, particularly in peptide chemistry. It serves as a key reagent for the protection of amino groups during peptide bond formation, ensuring selective reactions and high yields. Its application extends to the synthesis of complex peptides and proteins, where precise control over amino acid coupling is essential. Additionally, it is employed in the development of boron-based drugs, leveraging its unique properties to enhance drug stability and bioavailability. In medicinal chemistry, it plays a role in creating targeted therapies, especially for conditions like cancer and infectious diseases, by facilitating the incorporation of boron into biologically active molecules. Its chiral nature also makes it valuable in asymmetric synthesis, enabling the production of enantiomerically pure compounds for pharmaceutical applications.
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