Diphenyl 1-(Cbz-Amino)isobutylphosphonate
95%
- Product Code: 36120
CAS:
65164-83-2
Molecular Weight: | 439.4407 g./mol | Molecular Formula: | C₂₄H₂₆NO₅P |
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EC Number: | MDL Number: | MFCD03158925 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature |
Product Description:
Diphenyl 1-(Cbz-Amino)isobutylphosphonate is primarily used in organic synthesis, particularly in peptide chemistry. It serves as a key intermediate in the preparation of phosphonate-containing peptides, which are valuable in the development of enzyme inhibitors and bioactive molecules. The compound is often employed in the protection of amino groups during peptide synthesis, where the Cbz (carbobenzyloxy) group acts as a protective moiety. This allows for selective deprotection and further functionalization of the peptide chain. Additionally, its phosphonate group is useful in mimicking phosphate esters, making it relevant in studies involving phosphorylation and dephosphorylation processes in biological systems. Its applications extend to medicinal chemistry, where it aids in the design of potential therapeutic agents targeting enzymes and receptors.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | $186.51 |
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Diphenyl 1-(Cbz-Amino)isobutylphosphonate
Diphenyl 1-(Cbz-Amino)isobutylphosphonate is primarily used in organic synthesis, particularly in peptide chemistry. It serves as a key intermediate in the preparation of phosphonate-containing peptides, which are valuable in the development of enzyme inhibitors and bioactive molecules. The compound is often employed in the protection of amino groups during peptide synthesis, where the Cbz (carbobenzyloxy) group acts as a protective moiety. This allows for selective deprotection and further functionalization of the peptide chain. Additionally, its phosphonate group is useful in mimicking phosphate esters, making it relevant in studies involving phosphorylation and dephosphorylation processes in biological systems. Its applications extend to medicinal chemistry, where it aids in the design of potential therapeutic agents targeting enzymes and receptors.
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