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Catalog Number:
31697
CAS Number:
864876-94-8
Fmoc-L-Asp(OtBu)-O-CH2-Ph-OCH2-CH2-COOH
Purity:
≥ 99,5 % (HPLC chirale)
Documents
$72.31 /1G
Taille
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Product Information

Fmoc-L-Asp(OtBu)-O-CH2-Ph-OCH2-CH2-COOH is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a protective Fmoc (9-fluorenylmethoxycarbonyl) group, which is essential for the selective protection of the amino group during the synthesis of peptides. Its unique structure, which includes a t-butyl ester and a phenyl ether, enhances its stability and solubility, making it an excellent choice for researchers working on complex peptide sequences.

In the pharmaceutical industry, this compound is particularly valuable for the synthesis of bioactive peptides and can serve as a building block in the development of therapeutic agents. Its ability to facilitate the formation of peptide bonds while maintaining the integrity of sensitive functional groups makes it a preferred choice among chemists. Additionally, its application in solid-phase peptide synthesis allows for efficient and high-yield production of peptides, which are crucial in drug discovery and development processes.

CAS Number
864876-94-8
Purity
≥ 99,5 % (HPLC chirale)
Molecular Formula
C 33 H 359
Molecular Weight
589.64
MDL Number
MFCD08457845
PubChem ID
155893929
Appearance
Poudre blanche
Optical Rotation
[a] 20 D = -14 ± 2 ° (C = 1 dans DMF)
Conditions
Conserver à 0 - 8 °C
General Information
CAS Number
864876-94-8
Purity
≥ 99,5 % (HPLC chirale)
Molecular Formula
C 33 H 359
Molecular Weight
589.64
MDL Number
MFCD08457845
PubChem ID
155893929
Appearance
Poudre blanche
Optical Rotation
[a] 20 D = -14 ± 2 ° (C = 1 dans DMF)
Conditions
Conserver à 0 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fmoc-L-Asp(OtBu)-O-CH2-Ph-OCH2-CH2-COOH is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in solid-phase peptide synthesis, allowing for the selective modification of amino acids without interfering with other functional groups.
  • Drug Development: It plays a crucial role in the design of peptide-based therapeutics, particularly in targeting specific biological pathways, enhancing drug efficacy and selectivity.
  • Bioconjugation: The compound is used in bioconjugation processes, enabling the attachment of peptides to various biomolecules, which is essential in creating targeted drug delivery systems.
  • Research in Cancer Therapy: Its applications extend to cancer research, where it aids in the development of peptide drugs that can selectively target cancer cells, minimizing side effects.
  • Diagnostic Tools: The chemical is also utilized in the creation of diagnostic agents that can bind to specific biomarkers, improving the accuracy of disease detection.

Citations