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Catalog Number:
05467
CAS Number:
84888-35-7
Boc-S-9-fluorenylmethyl-L-cysteine
Purity:
≥ 99% (HPLC)
Synonym(s):
Boc-L-Cys(Fm)-OH
Documents
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Product Information

Boc-S-9-fluorenylmethyl-L-cysteine is a versatile compound widely utilized in peptide synthesis and drug development. This protected cysteine derivative features a fluorenylmethyl group, enhancing its stability and solubility, making it an ideal choice for researchers focused on synthesizing complex peptides. Its unique structure allows for selective reactions, facilitating the incorporation of sulfur-containing amino acids into peptides, which is crucial for developing therapeutics with improved bioactivity and stability.

In the pharmaceutical industry, Boc-S-9-fluorenylmethyl-L-cysteine is particularly valuable for creating peptide-based drugs, where the protection of functional groups is essential for maintaining the integrity of the final product. Additionally, its application in the synthesis of cyclic peptides and other bioactive compounds highlights its importance in medicinal chemistry. Researchers benefit from its ease of use and the ability to streamline synthesis processes, ultimately leading to more efficient drug development pathways.

Synonyms
Boc-L-Cys(Fm)-OH
CAS Number
84888-35-7
Purity
≥ 99% (HPLC)
Molecular Formula
C22H25NO4S
Molecular Weight
399.51
MDL Number
MFCD00076921
PubChem ID
18968128
Appearance
White powder or off-white solid
Conditions
Store at 0-8 °C
General Information
Synonyms
Boc-L-Cys(Fm)-OH
CAS Number
84888-35-7
Purity
≥ 99% (HPLC)
Molecular Formula
C22H25NO4S
Molecular Weight
399.51
MDL Number
MFCD00076921
PubChem ID
18968128
Appearance
White powder or off-white solid
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-9-fluorenylmethyl-L-cysteine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, particularly those containing cysteine. Its protective group allows for selective reactions, enhancing the efficiency of peptide assembly.
  • Drug Development: Researchers use this chemical in the development of new pharmaceuticals, especially in creating compounds that target specific biological pathways. Its unique structure can help in designing more effective drugs with fewer side effects.
  • Bioconjugation: The compound is instrumental in bioconjugation processes, where it can facilitate the attachment of drugs or imaging agents to proteins or antibodies, improving the delivery and efficacy of therapeutic agents.
  • Research in Protein Engineering: It is used in studies aimed at modifying proteins to enhance their stability or activity. This application is crucial in biotechnology and therapeutic protein production.
  • Analytical Chemistry: The compound can be utilized in analytical methods to study the interactions of cysteine-containing peptides, providing insights into their behavior in biological systems.

Citations