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Catalog Number:
33464
CAS Number:
2250436-46-3
Fmoc-L-Dap(2-Boc-aminoetil)-OH
Purity:
≥ 99 % (HPLC)
Synonym(s):
Fmoc-azalisina (Boc), N α-Fmoc- N ε-Boc-4-azalisina
Documents
$181.67 /25 mg
Tamaño
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Product Information

Fmoc-L-Dap(2-Boc-aminoethyl)-OH is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino groups during the synthesis of complex peptides. Its unique structure, including the Boc (tert-butyloxycarbonyl) group, enhances its stability and solubility, making it an excellent choice for researchers focused on synthesizing peptides with high purity and yield.

In practical applications, Fmoc-L-Dap(2-Boc-aminoethyl)-OH is particularly valuable in the development of peptide-based therapeutics and in the study of protein interactions. Its ability to facilitate the formation of peptide bonds while maintaining the integrity of the amino acid sequence allows for the creation of novel compounds with potential pharmaceutical applications. Researchers in the fields of medicinal chemistry and biochemistry will find this compound indispensable for advancing their work in peptide synthesis and drug discovery.

Synonyms
Fmoc-azalisina (Boc), N α-Fmoc- N ε-Boc-4-azalisina
CAS Number
2250436-46-3
Purity
≥ 99 % (HPLC)
Molecular Formula
C25H31N3O6
Molecular Weight
469.5
MDL Number
MFCD31380705
PubChem ID
170999912
Melting Point
152 - 154 °C (diciembre)
Appearance
Polvo cristalino blanco
Optical Rotation
[a] 20 D
Conditions
Conservar entre 2 y 8 °C.
General Information
Synonyms
Fmoc-azalisina (Boc), N α-Fmoc- N ε-Boc-4-azalisina
CAS Number
2250436-46-3
Purity
≥ 99 % (HPLC)
Molecular Formula
C25H31N3O6
Molecular Weight
469.5
MDL Number
MFCD31380705
PubChem ID
170999912
Melting Point
152 - 154 °C (diciembre)
Appearance
Polvo cristalino blanco
Optical Rotation
[a] 20 D
Conditions
Conservar entre 2 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

Fmoc-L-Dap(2-Boc-aminoethyl)-OH 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 activities.
  • Drug Development: It plays a crucial role in the development of new pharmaceuticals, particularly in designing peptide-based drugs that target specific diseases.
  • Bioconjugation: The compound is used in bioconjugation processes, enabling the attachment of biomolecules to drugs or imaging agents, enhancing their efficacy and targeting capabilities.
  • Research in Cancer Therapy: Researchers utilize this chemical to develop targeted therapies that can selectively attack cancer cells, improving treatment outcomes while minimizing side effects.
  • Diagnostics: It is applied in the creation of diagnostic tools, such as biosensors, that can detect specific biomarkers, aiding in early disease detection and monitoring.

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