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Catalog Number:
01989
Boc-S-acetamidomethyl-L-cysteine 4-oxymethylphenylacetamidomethyl resin
Synonym(s):
Boc-L-Cys(Acm)-PAM resin
Documents
$18.53 /1G
Pack Size Availability Price
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Product Information

Boc-S-acetamidomethyl-L-cysteine 4-oxymethylphenylacetamidomethyl is a versatile compound widely utilized in peptide synthesis and pharmaceutical research. This compound features a Boc (tert-butyloxycarbonyl) protecting group, which is essential for the selective protection of amines during chemical reactions. Its unique structure allows for the incorporation of sulfur-containing amino acids, making it particularly valuable in the development of bioactive peptides and drug candidates. Researchers appreciate its stability and compatibility with various coupling reagents, facilitating efficient synthesis processes.

In addition to its role in peptide synthesis, Boc-S-acetamidomethyl-L-cysteine 4-oxymethylphenylacetamidomethyl has potential applications in the development of targeted therapies and diagnostic agents. Its ability to form disulfide bonds can enhance the stability and efficacy of therapeutic peptides, making it a crucial component in the design of novel pharmaceuticals. With its favorable properties and diverse applications, this compound stands out as a key ingredient for researchers and industry professionals focused on advancing drug development and peptide chemistry.

Synonyms
Boc-L-Cys(Acm)-PAM resin
MDL Number
MFCD00801167
Substitution
0.3-0.8 meq/g
Mesh Size
100-200 mesh
Conditions
Store at 0-8°C
%DVB
1% DVB
General Information
Synonyms
Boc-L-Cys(Acm)-PAM resin
MDL Number
MFCD00801167
Substitution
0.3-0.8 meq/g
Mesh Size
100-200 mesh
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

Boc-S-acetamidomethyl-L-cysteine 4-oxymethylphenylacetamidomethyl is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for selective reactions without interfering with other functional groups.
  • Drug Development: It plays a crucial role in the development of pharmaceuticals, particularly in creating compounds that target specific biological pathways.
  • Bioconjugation: The compound is used in bioconjugation techniques, facilitating the attachment of biomolecules to surfaces or other molecules for enhanced functionality.
  • Research in Cancer Therapeutics: It is applied in studies aimed at developing targeted therapies for cancer, helping to create more effective treatment options.
  • Diagnostics: This chemical is involved in the formulation of diagnostic agents, improving the accuracy of disease detection and monitoring.

Citations