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Catalog Number:
02593
CAS Number:
198470-36-9
Boc-S-4-methylbenzyl-D-penicillamine dicyclohexylammonium salt
Purity:
≥ 98
Synonym(s):
Boc-D-Pen(pMeBzl)-OH·DCHA, Boc-β,β-dimethyl-D-Cys(pMeBzl)-OH·DCHA
Documents
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Product Information

Boc-S-4-methylbenzyl-D-penicillamine dicyclohexylammonium salt is a versatile compound recognized for its unique properties and applications in various fields, particularly in medicinal chemistry and pharmaceutical research. This compound serves as a valuable building block in the synthesis of peptide-based drugs, where its protective Boc (tert-butyloxycarbonyl) group allows for selective functionalization. Researchers appreciate its ability to facilitate the development of novel therapeutics, especially in the context of targeting specific biological pathways.

Additionally, Boc-S-4-methylbenzyl-D-penicillamine dicyclohexylammonium salt exhibits significant potential in the study of metal ion chelation, which is crucial for developing treatments for metal toxicity and related disorders. Its structural features enhance its reactivity and selectivity, making it an attractive candidate for further exploration in drug design and development. This compound not only streamlines synthetic processes but also opens avenues for innovative research in the pharmaceutical industry.

Synonyms
Boc-D-Pen(pMeBzl)-OH·DCHA, Boc-β,β-dimethyl-D-Cys(pMeBzl)-OH·DCHA
CAS Number
198470-36-9
Purity
≥ 98
Molecular Formula
C18H27NO4S·C12H23N
Molecular Weight
534.7
MDL Number
MFCD00235908
Conditions
Store at 0-8°C
General Information
Synonyms
Boc-D-Pen(pMeBzl)-OH·DCHA, Boc-β,β-dimethyl-D-Cys(pMeBzl)-OH·DCHA
CAS Number
198470-36-9
Purity
≥ 98
Molecular Formula
C18H27NO4S·C12H23N
Molecular Weight
534.7
MDL Number
MFCD00235908
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Boc-S-4-methylbenzyl-D-penicillamine dicyclohexylammonium salt is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for the selective modification of amino acids without affecting others. This is crucial for researchers developing complex peptide-based drugs.
  • Drug Development: It plays a role in the formulation of novel pharmaceuticals, particularly in the development of drugs targeting specific diseases, due to its unique structural properties that enhance bioavailability.
  • Bioconjugation: The compound is used in bioconjugation techniques, enabling the attachment of biomolecules to drugs or imaging agents, which is essential in targeted therapy and diagnostics in the medical field.
  • Research in Organosulfur Chemistry: It is a valuable reagent in studies involving organosulfur compounds, contributing to advancements in organic synthesis and materials science.
  • Antioxidant Studies: The compound is investigated for its potential antioxidant properties, which can lead to applications in food preservation and health supplements, offering benefits over traditional antioxidants.

Citations