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162558-25-0

L-Alanine, 3-[[(1,1-dimethylethoxy)carbonyl]amino]-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-

Catalog#: AR001TXK  |   CAS#: 162558-25-0  |   MDL#: MFCD00235896  |   MF: C23H26N2O6  |   MW: 426.4623

Packsize Purity Price Availability Quantity
250mg 97% $5.00 Global Stock Buy Now Add To Cart
1g 97% $5.00 Global Stock Buy Now Add To Cart
5g 97% $18.00 Global Stock Buy Now Add To Cart
10g 97% $33.00 Global Stock Buy Now Add To Cart
25g 97% $74.00 Global Stock Buy Now Add To Cart
100g 97% $262.00 Global Stock Buy Now Add To Cart
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Catalog Number AR001TXK
Chemical Name L-Alanine, 3-[[(1,1-dimethylethoxy)carbonyl]amino]-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-
CAS Number 162558-25-0
Molecular Formula C23H26N2O6
Molecular Weight 426.4623
MDL Number MFCD00235896
SMILES O=C(N[C@H](C(=O)O)CNC(=O)OC(C)(C)C)OCC1c2ccccc2c2c1cccc2

The N-Fmoc-N'-Boc-L-2,3-Diaminopropionic acid is a versatile building block widely utilized in chemical synthesis, particularly in the field of peptide chemistry. This amino acid derivative serves as a crucial component in the synthesis of complex peptides and peptidomimetics due to its unique structure and reactivity.One key application of N-Fmoc-N'-Boc-L-2,3-Diaminopropionic acid is in solid-phase peptide synthesis (SPPS). By incorporating this compound into the peptide chain, chemists can introduce specific functional groups and tailor the properties of the peptide to achieve desired biological activities or structural features. The Fmoc and Boc protecting groups provide temporary shielding of reactive sites during the synthesis process, enabling selective and controlled peptide bond formation.Furthermore, N-Fmoc-N'-Boc-L-2,3-Diaminopropionic acid can be utilized in the construction of peptidomimetics, which are compounds designed to mimic the structure and function of peptides. These mimetics often exhibit improved stability, bioavailability, and target specificity compared to natural peptides, making them valuable tools in drug discovery and development.Overall, the strategic incorporation of N-Fmoc-N'-Boc-L-2,3-Diaminopropionic acid in chemical synthesis enables researchers to access a diverse range of peptide-based molecules with tailored properties and functions, driving advancements in fields such as medicinal chemistry, biotechnology, and materials science.
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GHS Pictogram
Signal Word Warning
UN# N/A
Hazard Statements H302-H315-H319-H332-H335
Precautionary Statements P261-P280-P305+P351+P338
Class N/A
Packing Group N/A

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