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Catalog Number:
03980
CAS Number:
135592-14-2
Boc-S-trityl-D-penicillamine
Purity:
≥ 99% (HPLC)
Synonym(s):
Boc-D-Pen(Trt)-OH, Boc-β,β-dimethyl-D-Cys(Trt)-OH
Documents
$62.29 /250MG
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Product Information

Boc-S-trityl-D-penicillamine is a specialized compound widely utilized in the field of medicinal chemistry and peptide synthesis. This compound is recognized for its unique protective group, which enhances the stability and reactivity of thiol groups in various chemical reactions. Its structure allows for selective modifications, making it an invaluable tool for researchers engaged in the development of novel therapeutics and biologically active molecules.

In practical applications, Boc-S-trityl-D-penicillamine is often employed in the synthesis of peptide-based drugs and as a building block in the creation of complex organic compounds. Its ability to facilitate the introduction of sulfur-containing functionalities makes it particularly advantageous in the design of inhibitors and other bioactive agents. Researchers appreciate its compatibility with various coupling reactions, which streamlines the synthesis process and improves yields. This compound stands out for its versatility and effectiveness in advancing drug discovery and development efforts.

Synonyms
Boc-D-Pen(Trt)-OH, Boc-β,β-dimethyl-D-Cys(Trt)-OH
CAS Number
135592-14-2
Purity
≥ 99% (HPLC)
Molecular Formula
C29H33NO4S
Molecular Weight
491.6
MDL Number
MFCD00237382
PubChem ID
19807089
Melting Point
124-128? C
Optical Rotation
-48.0±1º (c=1 in MeOH)
Conditions
Store at 0-8°C
General Information
Synonyms
Boc-D-Pen(Trt)-OH, Boc-β,β-dimethyl-D-Cys(Trt)-OH
CAS Number
135592-14-2
Purity
≥ 99% (HPLC)
Molecular Formula
C29H33NO4S
Molecular Weight
491.6
MDL Number
MFCD00237382
PubChem ID
19807089
Melting Point
124-128? C
Optical Rotation
-48.0±1º (c=1 in MeOH)
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-S-trityl-D-penicillamine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing chemists to selectively modify amino acids without affecting others, enhancing the efficiency of drug development.
  • Drug Development: Its unique structure makes it valuable in designing novel therapeutics, particularly in the development of anti-cancer and anti-viral agents, where specificity and efficacy are crucial.
  • Bioconjugation: The compound is used to create bioconjugates, which are essential in targeted drug delivery systems. This application improves the therapeutic index of drugs by directing them to specific tissues.
  • Research in Enzyme Inhibition: It plays a role in studying enzyme inhibitors, providing insights into biochemical pathways and potential treatments for various diseases, including metabolic disorders.
  • Analytical Chemistry: Boc-S-trityl-D-penicillamine is employed in analytical techniques to detect and quantify thiol-containing compounds, aiding in quality control and research applications in pharmaceuticals.

Citations