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Catalog Number:
16833
CAS Number:
1176648-58-0
Fmoc-( S -2-méthoxyphénylglycine
Purity:
≥ 99 % (HPLC)
Synonym(s):
( Acide S- (Fmoc-amino)-(2-méthoxyphényl)acétique
Documents
$135.00 /100 mg
Taille
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Product Information

Fmoc-(S)-2-methoxyphenylglycine 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 allows for enhanced stability and solubility, making it an ideal choice for researchers in the fields of medicinal chemistry and biochemistry.

The compound's applications extend to the development of pharmaceuticals, particularly in the creation of peptide-based therapeutics. Its ability to facilitate the synthesis of bioactive peptides can lead to the discovery of novel drugs with improved efficacy and specificity. Additionally, Fmoc-(S)-2-methoxyphenylglycine is recognized for its role in the production of peptide libraries, which are crucial for high-throughput screening in drug discovery. By choosing this compound, researchers can benefit from its reliable performance and compatibility with various coupling reagents, ensuring successful peptide synthesis.

Synonyms
( Acide S- (Fmoc-amino)-(2-méthoxyphényl)acétique
CAS Number
1176648-58-0
Purity
≥ 99 % (HPLC)
Molecular Formula
C 24 H 215
Molecular Weight
403.43
MDL Number
MFCD07371754
PubChem ID
46737300
Appearance
Poudre blanche
Optical Rotation
[a] D 25 = +83,5 ± 6º (C = 1 dans DMF)
Conditions
Conserver à 0-8 °C
Safety & Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
General Information
Synonyms
( Acide S- (Fmoc-amino)-(2-méthoxyphényl)acétique
CAS Number
1176648-58-0
Purity
≥ 99 % (HPLC)
Molecular Formula
C 24 H 215
Molecular Weight
403.43
MDL Number
MFCD07371754
PubChem ID
46737300
Appearance
Poudre blanche
Optical Rotation
[a] D 25 = +83,5 ± 6º (C = 1 dans DMF)
Conditions
Conserver à 0-8 °C
Safety & Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Properties
Additional property information coming soon!
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Applications

Fmoc-(S)-2-methoxyphenylglycine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, enabling researchers to create complex structures for various applications in drug development.
  • Medicinal Chemistry: Its unique properties make it valuable in the design of new pharmaceuticals, particularly in targeting specific biological pathways, enhancing efficacy and reducing side effects.
  • Bioconjugation: The compound is used in bioconjugation processes, allowing scientists to attach biomolecules to surfaces or other molecules, which is crucial for developing targeted therapies and diagnostics.
  • Research in Neuroscience: It plays a role in studying neurotransmitter systems, helping researchers understand the mechanisms of action for potential neuroprotective agents.
  • Development of Drug Delivery Systems: Its properties facilitate the formulation of drug delivery systems that improve the bioavailability and stability of therapeutic agents.

Citations