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Catalog Number:
03977
CAS Number:
129972-45-8
Boc -S- acetamidometil-L-penicilamina
Purity:
≥ 99 % (TLC)
Synonym(s):
Boc-L-Pen(Acm)-OH, Boc- S -acetamidometil-β,β-dimetil-L-Cys-OH
Documents
$113.87 /1G
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Product Information

Boc-S-acetamidomethyl-L-penicillamine is a versatile compound widely utilized in the field of medicinal chemistry and peptide synthesis. This compound, known for its unique thiol group, serves as a valuable building block in the development of various pharmaceuticals and biologically active molecules. Its ability to form stable complexes with metal ions makes it particularly useful in the design of metallodrugs and chelating agents. Researchers appreciate its role in the synthesis of peptide derivatives, where it can enhance the stability and bioactivity of the resulting compounds.

In addition to its applications in drug development, Boc-S-acetamidomethyl-L-penicillamine is also employed in the study of protein interactions and enzyme inhibition. Its distinctive structural features allow for modifications that can lead to improved therapeutic profiles. This compound stands out among similar agents due to its favorable solubility and reactivity, making it an ideal choice for researchers aiming to explore new therapeutic avenues. With its broad range of applications, Boc-S-acetamidomethyl-L-penicillamine is an essential tool for professionals in pharmaceutical research and development.

Synonyms
Boc-L-Pen(Acm)-OH, Boc- S -acetamidometil-β,β-dimetil-L-Cys-OH
CAS Number
129972-45-8
Purity
≥ 99 % (TLC)
Molecular Formula
C13H24N2O5S
Molecular Weight
320.35
MDL Number
MFCD00151885
PubChem ID
14755064
Appearance
Polvo blanco
Optical Rotation
-14±1º (c=1% en MeOH)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Boc-L-Pen(Acm)-OH, Boc- S -acetamidometil-β,β-dimetil-L-Cys-OH
CAS Number
129972-45-8
Purity
≥ 99 % (TLC)
Molecular Formula
C13H24N2O5S
Molecular Weight
320.35
MDL Number
MFCD00151885
PubChem ID
14755064
Appearance
Polvo blanco
Optical Rotation
-14±1º (c=1% en MeOH)
Conditions
Conservar entre 0 y 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-acetamidomethyl-L-penicillamine 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. This is crucial in developing complex peptides for pharmaceuticals.
  • Drug Development: It plays a role in the design of new drugs, particularly in the field of antibiotics and antiviral agents, by modifying existing compounds to enhance their efficacy and reduce side effects.
  • Bioconjugation: The compound is used in bioconjugation processes, where it helps attach biomolecules to surfaces or other molecules, improving the delivery and targeting of therapeutic agents in medical applications.
  • Research in Biochemistry: It aids researchers in studying protein interactions and enzyme functions, providing insights into biochemical pathways that can lead to new therapeutic strategies.
  • Analytical Chemistry: The compound is employed in analytical methods to detect and quantify specific biomolecules, enhancing the accuracy of biochemical assays and diagnostics.

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