N-Boc-Tran-4-Fluoro-L-proline CAS: 203866-14-2
Catalog Number | XD94133 |
Product Name | N-Boc-Tran-4-Fluoro-L-proline |
CAS | 203866-14-2 |
Molecular Formula | C10H16FNO4 |
Molecular Weight | 233.24 |
Storage Details | Ambient |
Product Specification
Appearance | White powder |
Assay | 99% min |
N-Boc-Tran-4-Fluoro-L-proline is a chemical compound that finds application in organic synthesis and pharmaceutical research due to its unique properties and potential therapeutic benefits.One significant use of N-Boc-Tran-4-Fluoro-L-proline is in the synthesis of peptide analogs and mimetics. Peptides are essential molecules involved in various biological processes and have significant potential as therapeutic agents. The addition of a fluorine atom to the proline amino acid can enhance the bioactivity, stability, and pharmacokinetic properties of peptides. N-Boc-Tran-4-Fluoro-L-proline acts as an intermediate in the construction of peptide analogs, allowing researchers to modify and optimize peptide structures for improved drug-like properties.Furthermore, N-Boc-Tran-4-Fluoro-L-proline is used in the synthesis of small organic molecules with diverse biological activities. Fluorine substitution at specific positions in organic molecules can significantly alter their properties, including lipophilicity, metabolic stability, and receptor binding affinity. Incorporation of N-Boc-Tran-4-Fluoro-L-proline into the structural framework of small molecules can lead to compounds with enhanced potency or selectivity for specific biological targets. This makes N-Boc-Tran-4-Fluoro-L-proline a valuable tool for medicinal chemists in the development of novel drug candidates.N-Boc-Tran-4-Fluoro-L-proline is also employed in the synthesis of cyclic compounds, including heterocyclic and peptidomimetic scaffolds. Heterocycles, which contain atoms other than carbon in their rings, are significant components of pharmaceuticals and biologically active compounds. The introduction of a fluorine atom can enhance the properties of these heterocyclic compounds, making them more suitable for drug discovery efforts.The N-Boc protecting group in N-Boc-Tran-4-Fluoro-L-proline provides stability during synthesis, enabling chemists to manipulate and modify the compound while protecting other reactive sites. This ensures high yields and efficient chemical transformations during the synthesis process.In summary, N-Boc-Tran-4-Fluoro-L-proline is a versatile compound that has various applications in organic synthesis and pharmaceutical research. Its use in peptide analog synthesis, small molecule modification, and heterocyclic compound construction provides avenues for the development of new therapeutic agents. With its unique properties and potential for enhancing biological activity, N-Boc-Tran-4-Fluoro-L-proline offers valuable opportunities for drug discovery and development.