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65710-58-9

Boc-Dap(Z)-OH.DCHA

Catalog#: AR003P5B  |   CAS#: 65710-58-9  |   MDL#: MFCD00236880  |   MF: C28H45N3O6  |   MW: 519.6734

Packsize Purity Price Availability Quantity
1g 98% $11.00 Global Stock Buy Now Add To Cart
5g 98% $19.00 Global Stock Buy Now Add To Cart
25g 98% $91.00 Global Stock Buy Now Add To Cart
100g 98% $356.00 Global Stock Buy Now Add To Cart
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Catalog Number AR003P5B
Chemical Name Boc-Dap(Z)-OH.DCHA
CAS Number 65710-58-9
Molecular Formula C28H45N3O6
Molecular Weight 519.6734
MDL Number MFCD00236880
SMILES C1CCC(CC1)NC1CCCCC1.O=C(OCc1ccccc1)NC[C@@H](C(=O)O)NC(=O)OC(C)(C)C

Boc-Dap(Z)-OH.DCHA is a specialized compound widely utilized in chemical synthesis as a key building block in peptide chemistry. This compound, with its Boc (tert-butoxycarbonyl) and Dap(Z) (2,3-diaminopropionic acid with a Z protecting group) moieties, offers unique properties and functionalities that play a crucial role in peptide synthesis.Specifically, Boc-Dap(Z)-OH.DCHA is commonly employed in solid-phase peptide synthesis (SPPS) to introduce the Dap(Z) amino acid residue into peptide chains. The Boc protecting group safeguards the amino group during the synthesis process, ensuring selective reactions at the desired sites. The DCHA (N,N-diisopropylcarbodiimide, hydroxybenzotriazole) coupling reagent facilitates efficient peptide bond formation, enabling the sequential assembly of amino acids to construct complex peptides.Furthermore, the presence of the Z protecting group on the Dap residue allows for orthogonal deprotection strategies, enabling precise control over the removal of protecting groups at specific stages of peptide elongation. This strategic manipulability enhances the synthetic flexibility and versatility of Boc-Dap(Z)-OH.DCHA in the construction of diverse peptides with tailored properties and functions.Overall, Boc-Dap(Z)-OH.DCHA is a vital component in the chemical toolbox of peptide chemists, enabling the efficient synthesis of intricate peptide structures with high purity and precision. Its role in facilitating selective reactions, controlling protection and deprotection steps, and promoting robust peptide bond formation underscores its significance in advancing research and development in peptide-based therapeutics, diagnostics, and materials science applications.
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GHS Pictogram
Signal Word Warning
UN# N/A
Hazard Statements H302-H315-H319-H335
Precautionary Statements P261-P305+P351+P338
Class N/A
Packing Group N/A

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