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Catalog Number:
05561
CAS Number:
125602-26-8
Boc-Nα-methyl-Nω-(4-methoxy-2,3,6-trimethylbenzenesulfonyl)-L-arginine
Purity:
≥ 98% (HPLC)
Synonym(s):
Boc-N-Me-L-Arg(Mtr)-OH
Documents
$86.23 /250MG
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Product Information

Boc-Na-methyl-Nw-(4-methoxy-2,3,6-trimethylbenzenesulfonyl)-L-arginine is a sophisticated compound widely utilized in peptide synthesis and drug development. This compound features a unique sulfonyl group that enhances its reactivity and selectivity, making it an excellent choice for researchers focused on developing targeted therapies. Its distinctive structure allows for the modification of peptide sequences, facilitating the creation of novel therapeutic agents with improved efficacy and reduced side effects.

In the pharmaceutical industry, Boc-Na-methyl-Nw-(4-methoxy-2,3,6-trimethylbenzenesulfonyl)-L-arginine serves as a valuable building block in the synthesis of bioactive peptides, particularly those aimed at modulating biological pathways. Its ability to provide stability and protection during synthesis makes it a preferred choice among chemists. Additionally, its application in the development of peptide-based drugs highlights its potential in advancing therapeutic strategies for various diseases, including cancer and metabolic disorders.

Synonyms
Boc-N-Me-L-Arg(Mtr)-OH
CAS Number
125602-26-8
Purity
≥ 98% (HPLC)
Molecular Formula
C22H36N4O7S
Molecular Weight
500.62
MDL Number
MFCD00236863
PubChem ID
75193248
Appearance
White solid
Optical Rotation
[a]D20 = -38 ± 2º (C=0.55 in CHCl3)
Conditions
Store at 0-8°C
General Information
Synonyms
Boc-N-Me-L-Arg(Mtr)-OH
CAS Number
125602-26-8
Purity
≥ 98% (HPLC)
Molecular Formula
C22H36N4O7S
Molecular Weight
500.62
MDL Number
MFCD00236863
PubChem ID
75193248
Appearance
White solid
Optical Rotation
[a]D20 = -38 ± 2º (C=0.55 in CHCl3)
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Boc-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 protecting group in peptide synthesis, allowing for selective reactions without unwanted side reactions, which is crucial for creating complex peptides in pharmaceuticals.
  • Drug Development: It plays a role in the development of novel therapeutic agents, particularly in designing drugs that target specific biological pathways, enhancing efficacy and reducing side effects.
  • Bioconjugation: The compound is useful in bioconjugation techniques, where it can be attached to biomolecules for targeted drug delivery, improving the precision of treatments in cancer therapy.
  • Research in Enzyme Inhibition: It is applied in studies investigating enzyme inhibitors, particularly in the field of proteomics, helping researchers understand enzyme functions and develop inhibitors for diseases.
  • Analytical Chemistry: The compound is utilized in analytical methods to detect and quantify biomolecules, aiding researchers in characterizing biological samples with high specificity and sensitivity.

Citations