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Catalog Number:
05918
CAS Number:
84888-34-6
S-9-Fluorenylmethyl-L-cysteine hydrochloride
Purity:
≥ 99% (TLC)
Synonym(s):
L-Cys(Fm)-OH·HCl
Documents
$100.00 /250MG
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Product Information

S-9-Fluorenylmethyl-L-cysteine hydrochloride is a valuable compound widely utilized in the fields of biochemistry and pharmaceutical research. This compound, known for its unique structure, serves as a potent protecting group for thiol functionalities in peptide synthesis, enabling researchers to create complex molecules with enhanced stability and reactivity. Its ability to selectively protect cysteine residues makes it an essential tool in the development of peptide-based therapeutics and bioconjugates, facilitating the exploration of novel drug candidates.

In addition to its role in peptide synthesis, S-9-Fluorenylmethyl-L-cysteine hydrochloride has shown promise in various applications, including the study of protein interactions and the development of targeted delivery systems. Researchers appreciate its compatibility with a range of reaction conditions, which allows for versatile use in synthetic chemistry. With its unique properties and practical applications, this compound is an indispensable asset for professionals aiming to innovate in drug development and biochemical research.

Synonyms
L-Cys(Fm)-OH·HCl
CAS Number
84888-34-6
Purity
≥ 99% (TLC)
Molecular Formula
C17H17NO2S·HCl
Molecular Weight
335.88
MDL Number
MFCD00236944
PubChem ID
137795308
Appearance
White powder
Conditions
Store at 0-8 °C
General Information
Synonyms
L-Cys(Fm)-OH·HCl
CAS Number
84888-34-6
Purity
≥ 99% (TLC)
Molecular Formula
C17H17NO2S·HCl
Molecular Weight
335.88
MDL Number
MFCD00236944
PubChem ID
137795308
Appearance
White powder
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

S-9-Fluorenylmethyl-L-cysteine hydrochloride is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in peptide synthesis, allowing chemists to selectively modify amino acids without affecting the overall structure. It enhances the efficiency of creating complex peptides used in pharmaceuticals.
  • Drug Development: Researchers leverage its properties to develop new drugs, particularly in the field of cancer research, where it aids in the design of molecules that can target specific pathways in tumor cells.
  • Bioconjugation: The compound is effective in bioconjugation processes, where it helps link biomolecules to therapeutic agents, improving the delivery and efficacy of treatments in areas like immunotherapy.
  • Analytical Chemistry: It is used as a standard in analytical methods, providing a reliable reference for quantifying other compounds in complex mixtures, which is crucial for quality control in pharmaceuticals.
  • Research in Protein Engineering: This chemical plays a role in modifying proteins to study their functions and interactions, aiding advancements in biotechnology and synthetic biology.

Citations