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Catalog Number:
02819
Fmoc-S-trityl-L-cysteine 4-alkoxybenzyl alcohol resin
Synonym(s):
Fmoc-L-Cys(Trt)-Wang resin
Documents
$29.34 /1G
Pack Size Availability Price
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Product Information

Fmoc-S-trityl-L-cysteine 4-alkoxybenzyl alcohol is a versatile compound widely utilized in peptide synthesis and drug development. This compound features a unique combination of protective groups that facilitate the selective modification of cysteine residues in peptides, making it an essential tool for researchers in the fields of biochemistry and medicinal chemistry. Its ability to stabilize thiol groups while allowing for further functionalization enhances its utility in the synthesis of complex peptide structures, which are crucial for developing therapeutic agents and studying protein interactions.

In addition to its role in peptide synthesis, Fmoc-S-trityl-L-cysteine 4-alkoxybenzyl alcohol is also valuable in the design of novel biomaterials and drug delivery systems. Its functional groups can be easily modified to create tailored compounds that meet specific research needs. This compound stands out due to its stability and compatibility with various coupling reactions, making it a preferred choice for professionals seeking reliable and efficient solutions in their synthetic pathways.

Synonyms
Fmoc-L-Cys(Trt)-Wang resin
MDL Number
MFCD00801374
Appearance
Pale to yellow beads
Substitution
0.3-0.8 mmol/g
Mesh Size
200 - 400
Conditions
Store at 0-8 °C
%DVB
1% DVB
General Information
Synonyms
Fmoc-L-Cys(Trt)-Wang resin
MDL Number
MFCD00801374
Appearance
Pale to yellow beads
Substitution
0.3-0.8 mmol/g
Mesh Size
200 - 400
Conditions
Store at 0-8 °C
%DVB
1% DVB
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-S-trityl-L-cysteine 4-alkoxybenzyl alcohol is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for selective functionalization of amino acids without unwanted reactions.
  • Drug Development: It plays a crucial role in the design of novel pharmaceuticals, particularly in creating compounds that target specific biological pathways.
  • Bioconjugation: The chemical is used to attach biomolecules to surfaces or other molecules, enhancing the development of biosensors and targeted drug delivery systems.
  • Research in Cancer Therapeutics: Its unique properties allow researchers to explore new treatments by modifying existing compounds to improve efficacy and reduce side effects.
  • Material Science: The compound is applied in the development of advanced materials, such as coatings and polymers, that require specific chemical functionalities for enhanced performance.

Citations