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Catalog Number:
07352
CAS Number:
79839-29-5
Boc-(3S-3-amino-1-carboxymethyl-caprolactame
Purity:
≥ 97% (NMR)
Documents
$100.05 /100MG
Pack Size Availability Price
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Product Information

Boc-(3S)-3-amino-1-carboxymethylcaprolactame is a versatile compound widely utilized in the fields of medicinal chemistry and peptide synthesis. This compound features a Boc (tert-butyloxycarbonyl) protecting group, which is essential for the selective protection of amines during synthetic processes. Its unique structure allows for the incorporation of amino acids into peptide chains, making it a valuable building block for researchers engaged in drug development and protein engineering.

The compound's stability and ease of handling make it particularly advantageous in laboratory settings, where precise control over reaction conditions is crucial. Its application extends to the synthesis of bioactive peptides, which are pivotal in therapeutic interventions. Additionally, Boc-(3S)-3-amino-1-carboxymethylcaprolactame can be employed in the development of novel drug candidates, enhancing the efficiency of pharmaceutical research. With its robust properties and practical applications, this compound stands out as a key resource for professionals in the chemical and pharmaceutical industries.

CAS Number
79839-29-5
Purity
≥ 97% (NMR)
Molecular Formula
C13H22N2O5
Molecular Weight
286.32
MDL Number
MFCD00673777
PubChem ID
4712529
Appearance
White powder
Optical Rotation
[a]D20 = +26 ± 3º (C=1 in CHCl3
Conditions
Store at 0-8 °C
General Information
CAS Number
79839-29-5
Purity
≥ 97% (NMR)
Molecular Formula
C13H22N2O5
Molecular Weight
286.32
MDL Number
MFCD00673777
PubChem ID
4712529
Appearance
White powder
Optical Rotation
[a]D20 = +26 ± 3º (C=1 in CHCl3
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Boc-(3S)-3-amino-1-carboxymethylcaprolactame is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in peptide synthesis, allowing for the selective modification of amino acids without interfering with other functional groups. This is crucial for developing complex peptides used in pharmaceuticals.
  • Drug Development: Its structure enables researchers to create novel drug candidates, particularly in the field of antibiotics and anticancer agents. The ability to modify the lactam ring enhances the compound's bioactivity and stability.
  • Bioconjugation: The compound can be used in bioconjugation techniques, linking biomolecules to drugs or imaging agents. This application is essential in targeted therapy and diagnostic imaging, improving treatment efficacy.
  • Research in Neuroscience: Its derivatives are explored for potential neuroprotective effects, making it a candidate for developing treatments for neurodegenerative diseases.
  • Material Science: The compound's unique properties allow it to be incorporated into polymers, enhancing material characteristics for applications in drug delivery systems and biomaterials.

Citations