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AI65497

97745-69-2 | Boc-Arg(Boc)2-OH

Packsize Purity Availability Price Discounted Price    Quantity
100mg 90% in stock $39.00 $27.00 -   +
250mg 90% in stock $76.00 $53.00 -   +
500mg 90% in stock $144.00 $101.00 -   +
1g 90% in stock $273.00 $191.00 -   +
5g 90% in stock $1,193.00 $835.00 -   +
25g 90% in stock $4,142.00 $2,900.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AI65497
Chemical Name: Boc-Arg(Boc)2-OH
CAS Number: 97745-69-2
Molecular Formula: C21H38N4O8
Molecular Weight: 474.5484199999999
MDL Number: MFCD09807206
SMILES: O=C(OC(C)(C)C)NC(=N)N(C(=O)OC(C)(C)C)CCC[C@@H](C(=O)O)NC(=O)OC(C)(C)C

 

Upstream Synthesis Route
  • The compound (S)-5-(1,3-Bis(tert-butoxycarbonyl)guanidino)-2-((tert-butoxycarbonyl)amino)pentanoic acid, also known as $name$, is a valuable building block in chemical synthesis. It is commonly used as a chiral intermediate in the production of peptides and other complex organic molecules.$name$ plays a crucial role in peptide synthesis by serving as a protected form of the amino acids it contains. Its tert-butoxycarbonyl (Boc) groups act as temporary protecting groups, allowing for selective reactions to occur at specific sites within the molecule. This controlled reactivity is essential for the stepwise assembly of peptides with high purity and precision.In addition, $name$ is particularly well-suited for the synthesis of peptides with multiple guanidino groups, as its structure includes a guanidino moiety that can facilitate the formation of peptide bonds and enhance the overall functionality of the target molecule.Overall, the strategic incorporation of $name$ into chemical synthesis pathways enables chemists to access a diverse array of peptide-based compounds with tailored structures and properties, making it an indispensable tool for modern organic synthesis strategies.
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