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Catalog Number:
37551
CAS Number:
1403834-74-1
N-α-Fmoc-S-2,4,6-trimethoxyphenylthio-L-cysteine
Purity:
≥ 97% (HPLC)
Synonym(s):
Fmoc-L-Cys(STmp)-OH
Documents
$85.00 /100MG
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Product Information

N-a-Fmoc-S-2,4,6-trimethoxyphenylthio-L-cysteine is a versatile compound widely utilized in peptide synthesis and bioconjugation applications. This protected cysteine derivative features a fluorenylmethoxycarbonyl (Fmoc) group, which provides stability during synthesis while allowing for selective deprotection. The presence of the trimethoxyphenylthio moiety enhances its reactivity, making it an excellent choice for the formation of disulfide bonds in peptide chains. Researchers in the fields of medicinal chemistry and biochemistry can leverage this compound for the development of peptide-based therapeutics and probes, facilitating studies in protein interactions and cellular signaling pathways.

This compound's unique structure not only aids in the synthesis of complex peptides but also offers advantages over similar compounds by providing enhanced solubility and stability. Its application extends to the creation of targeted drug delivery systems and the development of novel biomaterials. With its robust performance in various chemical reactions, N-a-Fmoc-S-2,4,6-trimethoxyphenylthio-L-cysteine stands out as a valuable tool for researchers aiming to innovate in peptide chemistry and related fields.

Synonyms
Fmoc-L-Cys(STmp)-OH
CAS Number
1403834-74-1
Purity
≥ 97% (HPLC)
Molecular Formula
C27H27NO7S2
Molecular Weight
541.64
MDL Number
MFCD27957369
PubChem ID
138108874
Appearance
White to off-white powder
Optical Rotation
[a]D20 = -83 ± 2 ° (C=1 in DCM)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Fmoc-L-Cys(STmp)-OH
CAS Number
1403834-74-1
Purity
≥ 97% (HPLC)
Molecular Formula
C27H27NO7S2
Molecular Weight
541.64
MDL Number
MFCD27957369
PubChem ID
138108874
Appearance
White to off-white powder
Optical Rotation
[a]D20 = -83 ± 2 ° (C=1 in DCM)
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

N-a-Fmoc-S-2,4,6-trimethoxyphenylthio-L-cysteine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis, enabling researchers to create complex molecules for various applications.
  • Drug Development: It plays a significant role in the design of novel therapeutics, especially in targeting specific proteins, which is crucial in the pharmaceutical industry for developing effective treatments.
  • Bioconjugation: The chemical is used in bioconjugation processes, allowing for the attachment of biomolecules to drugs or imaging agents, enhancing their efficacy and specificity in medical applications.
  • Research in Cancer Therapy: Its properties make it valuable in studies aimed at developing targeted cancer therapies, providing insights into how to effectively deliver drugs to tumor cells.
  • Antioxidant Studies: The compound is also explored for its antioxidant properties, contributing to research in fields such as nutrition and health, where it may help in formulating supplements that combat oxidative stress.

Citations