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Catalog Number:
06301
CAS Number:
161561-83-7
Acide N α - Boc- N β -allyloxycarbonyl-L-2,3-diaminopropionique
Purity:
98% (HPLC)
Synonym(s):
Boc-L-Dap(Aloc)-OH
Documents
$100.05 /1G
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Product Information

Na-Boc-Nb-allyloxycarbonyl-L-2,3-diaminopropionic acid is a versatile compound widely utilized in peptide synthesis and pharmaceutical research. This amino acid derivative features a protective Boc (tert-butyloxycarbonyl) group, which enhances its stability and facilitates its incorporation into various peptide sequences. Its unique structure allows for selective reactions, making it an ideal choice for researchers focused on developing novel therapeutics or studying complex biological processes.

In addition to its applications in synthetic chemistry, Na-Boc-Nb-allyloxycarbonyl-L-2,3-diaminopropionic acid serves as a valuable building block in the design of bioactive molecules. Its ability to undergo further functionalization opens up possibilities for creating targeted drug delivery systems and improving the efficacy of existing medications. Researchers in the fields of medicinal chemistry and biochemistry will find this compound particularly beneficial for advancing their projects and achieving innovative results.

Synonyms
Boc-L-Dap(Aloc)-OH
CAS Number
161561-83-7
Purity
98% (HPLC)
Molecular Formula
C12H21N2O6
Molecular Weight
288.38
MDL Number
MFCD00798611
PubChem ID
3593591
Melting Point
78 - 92 °C
Appearance
Poudre cristalline blanche
Optical Rotation
[a] D 20 = -10,5 à -12,5 º (C=1 dans MeOH)
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Boc-L-Dap(Aloc)-OH
CAS Number
161561-83-7
Purity
98% (HPLC)
Molecular Formula
C12H21N2O6
Molecular Weight
288.38
MDL Number
MFCD00798611
PubChem ID
3593591
Melting Point
78 - 92 °C
Appearance
Poudre cristalline blanche
Optical Rotation
[a] D 20 = -10,5 à -12,5 º (C=1 dans MeOH)
Conditions
Conserver à 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Na-Boc-Nb-allyloxycarbonyl-L-2,3-diaminopropionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing researchers to create complex structures with specific biological functions.
  • Drug Development: It plays a crucial role in the design of new pharmaceuticals, particularly in developing targeted therapies due to its ability to modify amino acids for enhanced bioactivity.
  • Bioconjugation: The compound is used in bioconjugation techniques, facilitating the attachment of biomolecules to surfaces or other molecules, which is essential in diagnostics and therapeutic applications.
  • Research in Neuroscience: Its derivatives are explored in neuroscience for their potential use in neuroprotective agents, helping to understand and treat neurodegenerative diseases.
  • Material Science: The compound is also investigated for its properties in creating novel materials, such as hydrogels, which have applications in drug delivery systems and tissue engineering.

Citations