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Home  > N2-[(Phenylmethoxy)carbonyl]-D-arginylglycyl-N-(4-nitrophenyl)-L-argininamide dihydrochloride

AE13125

113711-77-6 | N2-[(Phenylmethoxy)carbonyl]-D-arginylglycyl-N-(4-nitrophenyl)-L-argininamide dihydrochloride

Packsize Purity Availability Price Discounted Price    Quantity
1mg 98% in stock $63.00 $45.00 -   +
5mg 98% in stock $278.00 $195.00 -   +
10mg 98% in stock $458.00 $321.00 -   +
25mg 98% in stock $915.00 $640.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AE13125
Chemical Name: N2-[(Phenylmethoxy)carbonyl]-D-arginylglycyl-N-(4-nitrophenyl)-L-argininamide dihydrochloride
CAS Number: 113711-77-6
Molecular Formula: C28H41Cl2N11O7
Molecular Weight: 714.6006400000003
MDL Number: MFCD03093407
SMILES: NC(=N)NCCC[C@H](C(=O)NCC(=O)N[C@H](C(=O)Nc1ccc(cc1)[N+](=O)[O-])CCCNC(=N)N)NC(=O)OCc1ccccc1.Cl.Cl

 

Upstream Synthesis Route
  • The N2-[(Phenylmethoxy)carbonyl]-D-arginylglycyl-N-(4-nitrophenyl)-L-argininamide dihydrochloride is a valuable compound used in chemical synthesis for peptide bond formation and modification. Specifically, this compound serves as a protecting group for the arginine residue, allowing for selective deprotection during the synthesis process. By incorporating this dihydrochloride derivative into the peptide synthesis workflow, chemists can achieve precise control over the coupling and deprotection steps, leading to the production of high-quality peptides with desired sequences and functionalities. This compound plays a crucial role in facilitating the efficient and accurate assembly of complex peptide structures in organic synthesis applications.
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