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13726-76-6

L-Arginine, N2-[(1,1-dimethylethoxy)carbonyl]-

Catalog#: AR0013QG  |   CAS#: 13726-76-6  |   MDL#: MFCD00042632  |   MF: C11H22N4O4  |   MW: 274.3168

Packsize Purity Price Availability Quantity
1g 98% $4.00 Global Stock Buy Now Add To Cart
5g 98% $5.00 Global Stock Buy Now Add To Cart
10g 98% $8.00 Global Stock Buy Now Add To Cart
25g 98% $15.00 Global Stock Buy Now Add To Cart
100g 98% $54.00 Global Stock Buy Now Add To Cart
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Catalog Number AR0013QG
Chemical Name L-Arginine, N2-[(1,1-dimethylethoxy)carbonyl]-
CAS Number 13726-76-6
Molecular Formula C11H22N4O4
Molecular Weight 274.3168
MDL Number MFCD00042632
SMILES OC(=O)[C@@H](NC(=O)OC(C)(C)C)CCCNC(=N)N

(S)-2-((tert-Butoxycarbonyl)amino)-5-guanidinopentanoic acid, also known as $name$, serves a crucial role in chemical synthesis as a versatile building block for the preparation of peptide-based molecules. Its unique structure, incorporating a guanidine group and a tert-butoxycarbonyl (Boc) protecting group, makes it ideal for use in the synthesis of complex peptide sequences.In peptide synthesis, (S)-2-((tert-Butoxycarbonyl)amino)-5-guanidinopentanoic acid acts as a key intermediate for introducing guanidine functionality into the peptide chain, enabling the formation of peptide bonds and facilitating the assembly of peptides with specific sequences and structures. The Boc protecting group ensures that the guanidine moiety remains stable during the synthesis process, allowing for controlled and selective deprotection when required.Furthermore, the guanidine functionality of this compound imparts unique properties to the peptides that are synthesized using it, making them valuable in various biological and pharmaceutical applications. The presence of the guanidine group can enhance the binding affinity of peptides to target molecules, enabling the development of peptide-based therapeutics, inhibitors, and ligands with improved efficacy and specificity.Overall, (S)-2-((tert-Butoxycarbonyl)amino)-5-guanidinopentanoic acid plays a pivotal role in chemical synthesis by enabling the efficient construction of diverse peptide structures with tailored functionalities, opening up new possibilities for the design and development of novel bioactive compounds with significant potential in drug discovery and other chemical research endeavors.
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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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