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Catalog Number:
31702
CAS Number:
864876-93-7
Fmoc-L-Met-O-CH2-Ph-OCH2-CH2-COOH
Purity:
≥ 99.5% (Chiral HPLC)
Documents
$43.87 /1G
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Product Information

Fmoc-L-Met-O-CH2-Ph-OCH2-CH2-COOH is a versatile compound widely utilized in peptide synthesis and drug development. This amino acid derivative features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amines during the synthesis of peptides. Its unique structure allows for the incorporation of methionine into peptides, making it invaluable in the production of bioactive compounds and pharmaceuticals. Researchers and industry professionals appreciate its stability and ease of use, particularly in solid-phase peptide synthesis (SPPS), where it enhances the efficiency of the coupling reactions.

In addition to its role in peptide synthesis, Fmoc-L-Met-O-CH2-Ph-OCH2-CH2-COOH has potential applications in the development of targeted drug delivery systems and therapeutic agents. Its ability to form stable conjugates with various biomolecules opens avenues for innovative treatments in areas such as cancer therapy and regenerative medicine. The compound's favorable properties make it a preferred choice for researchers seeking reliable and effective building blocks for complex molecular architectures.

CAS Number
864876-93-7
Purity
≥ 99.5% (Chiral HPLC)
Molecular Formula
C30H31NO7S
Molecular Weight
549.64
MDL Number
MFCD08457851
PubChem ID
155893006
Appearance
White powder
Optical Rotation
[a]20D = -23 ± 1 º ( C=1 in DMF)
Conditions
Store at 0 - 8 °C
General Information
CAS Number
864876-93-7
Purity
≥ 99.5% (Chiral HPLC)
Molecular Formula
C30H31NO7S
Molecular Weight
549.64
MDL Number
MFCD08457851
PubChem ID
155893006
Appearance
White powder
Optical Rotation
[a]20D = -23 ± 1 º ( 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-Met-O-CH2-Ph-OCH2-CH2-COOH is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing for the selective modification of amino acids without affecting others. Its stability under various conditions makes it ideal for complex peptide sequences.
  • Drug Development: In pharmaceutical research, it is used to create prodrugs that enhance the bioavailability of active pharmaceutical ingredients. This can lead to more effective treatments with fewer side effects.
  • Bioconjugation: The compound is valuable in bioconjugation processes, where it helps link biomolecules to therapeutic agents. This application is crucial in developing targeted therapies in cancer treatment.
  • Material Science: It finds applications in creating functional materials, such as hydrogels, which can be used in drug delivery systems. These materials can release drugs in a controlled manner, improving therapeutic outcomes.
  • Research in Proteomics: The compound is utilized in proteomics studies to label and analyze proteins. This helps researchers understand protein interactions and functions, which is vital in many biological studies.

Citations