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62234-36-0

N-α-Z-N-β-Boc-D-2,3-diaminopropionic acid

Catalog#: AR00EBE1  |   CAS#: 62234-36-0  |   MDL#: MFCD01318749  |   MF: C16H22N2O6  |   MW: 338.3557

Packsize Purity Price Availability Quantity
250mg 97% $4.00 Global Stock Buy Now Add To Cart
1g 97% $9.00 Global Stock Buy Now Add To Cart
5g 97% $39.00 Global Stock Buy Now Add To Cart
10g 97% $67.00 Global Stock Buy Now Add To Cart
25g 97% $119.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00EBE1
Chemical Name N-α-Z-N-β-Boc-D-2,3-diaminopropionic acid
CAS Number 62234-36-0
Molecular Formula C16H22N2O6
Molecular Weight 338.3557
MDL Number MFCD01318749
SMILES O=C(N[C@@H](C(=O)O)CNC(=O)OC(C)(C)C)OCc1ccccc1

Z-D-Dap(Boc)-OH, also known as Nα-Boc-tert-butyl-oxy-carbonyl-Z-Diaminopropionic acid, is a versatile reagent commonly used in chemical synthesis for the modification and functionalization of peptides and other organic compounds. This compound serves as a strategic building block in peptide synthesis due to its ability to selectively protect the amino group of aspartic acid derivatives.In peptide synthesis, Z-D-Dap(Boc)-OH is typically used as a protected amino acid derivative to introduce the diastereomeric Z-configuration at the α-carbon. This protection strategy prevents unwanted reactions with other functional groups and ensures regioselective modifications at the specific site. Additionally, the Boc (tert-butoxycarbonyl) protecting group safeguards the amine functionality from premature deprotection, enabling sequential derivatization steps in peptide assembly processes.By utilizing Z-D-Dap(Boc)-OH in chemical synthesis, researchers can manipulate the stereochemistry of peptide chains, control the reactivity of amino acids, and enhance the overall efficiency of peptide coupling reactions. This reagent serves as a key tool for the construction of complex peptide structures with precise control over stereochemistry and functionality, making it indispensable in modern peptide chemistry and drug discovery endeavors.
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