(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 |
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| 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 | ฿640.00 |
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| 1.000 | 10-20 days | ฿2,280.00 |
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| 5.000 | 10-20 days | ฿8,120.00 |
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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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