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Catalog Number:
31701
CAS Number:
1356004-85-7
Fmoc-L-Lys(Boc)-O-CH2-Ph-OCH2-CH2-COOH
Purity:
≥ 99.5% (Chiral HPLC)
Documents
$72.31 /1G
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Product Information

Fmoc-L-Lys(Boc)-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-fluorenylmethyloxycarbonyl) group, which is essential for the selective protection of the amino group during the synthesis of peptides. Its Boc (tert-butyloxycarbonyl) group further enhances stability and solubility, making it an ideal choice for researchers working on complex peptide sequences. The unique structure of this compound allows for the introduction of various functional groups, facilitating the design of novel therapeutics and bioconjugates.

In practical applications, Fmoc-L-Lys(Boc)-O-CH2-Ph-OCH2-CH2-COOH is particularly valuable in the fields of medicinal chemistry and biochemistry. It can be employed in the synthesis of peptide-based drugs, where precise control over amino acid sequences is crucial for achieving desired biological activity. Additionally, its ability to form stable conjugates with other biomolecules opens up possibilities for targeted drug delivery systems. Researchers appreciate its ease of use and the efficiency it brings to peptide synthesis, making it a preferred choice in laboratories focused on innovative therapeutic solutions.

CAS Number
1356004-85-7
Purity
≥ 99.5% (Chiral HPLC)
Molecular Formula
C36H42N2O9
Molecular Weight
646.74
MDL Number
MFCD08457850
PubChem ID
155892637
Appearance
White powder
Optical Rotation
[a]20D = -12 ± 1 ° (C=1 in DMF)
Conditions
Store at 0 - 8 °C
General Information
CAS Number
1356004-85-7
Purity
≥ 99.5% (Chiral HPLC)
Molecular Formula
C36H42N2O9
Molecular Weight
646.74
MDL Number
MFCD08457850
PubChem ID
155892637
Appearance
White powder
Optical Rotation
[a]20D = -12 ± 1 ° (C=1 in DMF)
Conditions
Store at 0 - 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-Lys(Boc)-O-CH2-Ph-OCH2-CH2-COOH is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, which are essential for drug development and biological research. Its protective groups allow for selective reactions, making it easier to create complex peptide structures.
  • Drug Delivery Systems: The compound can be incorporated into drug delivery formulations, enhancing the stability and release profiles of therapeutic agents. This is particularly beneficial in targeted therapies where precise drug delivery is crucial.
  • Bioconjugation: It is used in bioconjugation techniques to attach biomolecules to surfaces or other molecules. This application is vital in creating biosensors and diagnostic tools that require high specificity and sensitivity.
  • Research in Cancer Therapeutics: The compound's structure allows for modifications that can improve the efficacy of anticancer agents, making it a valuable tool in the development of new cancer treatments.
  • Protein Engineering: It plays a significant role in protein engineering, where it can be used to modify amino acids in proteins, enhancing their stability and functionality for various applications in biotechnology.

Citations