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Catalog Number:
05742
CAS Number:
214750-72-8
Nα-Fmoc-Nα-methyl-Nω-(4-methoxy-2,3,6-trimethylbenzenesulfonyl)-L-arginine
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-N-Me-L-Arg(Mtr)-OH
Documents
$113.87 /100MG
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Product Information

Na-Fmoc-Na-methyl-Nw-(4-methoxy-2,3,6-trimethylbenzenesulfonyl)-L-arginine is a sophisticated amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a unique Fmoc (9-fluorenylmethoxycarbonyl) protecting group, which is essential for the selective protection of amino groups during the synthesis of peptides. Its sulfonyl group enhances the compound's reactivity and solubility, making it an attractive choice for researchers focused on developing complex peptide structures.

This compound is particularly valuable in the field of medicinal chemistry, where it can be employed in the design of peptide-based therapeutics. Its ability to facilitate the formation of stable peptide bonds while maintaining the integrity of sensitive functional groups allows for the creation of highly specific and effective drug candidates. Additionally, Na-Fmoc-Na-methyl-Nw-(4-methoxy-2,3,6-trimethylbenzenesulfonyl)-L-arginine can be utilized in various applications, including the synthesis of cyclic peptides and in the development of targeted delivery systems, showcasing its versatility and importance in contemporary research.

Synonyms
Fmoc-N-Me-L-Arg(Mtr)-OH
CAS Number
214750-72-8
Purity
≥ 98% (HPLC)
Molecular Formula
C32H38N4O7S
Molecular Weight
622.9
MDL Number
MFCD02094400
PubChem ID
75193251
Appearance
White to off-white powder
Conditions
Store at ≤ -15 °C
General Information
Synonyms
Fmoc-N-Me-L-Arg(Mtr)-OH
CAS Number
214750-72-8
Purity
≥ 98% (HPLC)
Molecular Formula
C32H38N4O7S
Molecular Weight
622.9
MDL Number
MFCD02094400
PubChem ID
75193251
Appearance
White to off-white powder
Conditions
Store at ≤ -15 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Na-Fmoc-Na-methyl-Nw-(4-methoxy-2,3,6-trimethylbenzenesulfonyl)-L-arginine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing researchers to create complex molecules for various biological studies.
  • Drug Development: It plays a crucial role in the pharmaceutical industry, particularly in the development of peptide-based drugs, enhancing the efficacy and specificity of therapeutic agents.
  • Bioconjugation: The compound is used in bioconjugation processes, where it helps attach biomolecules to surfaces or other molecules, improving the functionality of diagnostic tools and therapeutic agents.
  • Protein Engineering: Researchers leverage this chemical in protein engineering to modify protein structures, which can lead to the development of novel enzymes or therapeutic proteins with improved properties.
  • Research in Cancer Therapeutics: Its applications extend to cancer research, where it aids in the design of targeted therapies that can selectively attack cancer cells while minimizing damage to healthy tissues.

Citations