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Catalog Number:
29720
CAS Number:
1260616-59-8
Fmoc-L-3,4-diméthoxy-homophénylalanine
Purity:
≥ 98 % (HPLC)
Synonym(s):
( Acide S -Fmoc-2-amino-4-(3,4-diméthoxyphényl)-butyrique
Documents
$134.70 /25 mg
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Product Information

Fmoc-L-3,4-dimethoxy-homophenylalanine 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 peptides. Its unique structure, characterized by the presence of two methoxy groups on the aromatic ring, enhances its stability and solubility, making it an excellent choice for researchers in medicinal chemistry and biochemistry.

In practical applications, Fmoc-L-3,4-dimethoxy-homophenylalanine is particularly valuable in the development of bioactive peptides, which can serve as therapeutic agents or research tools. Its ability to facilitate the formation of peptide bonds while maintaining the integrity of sensitive functional groups allows for the creation of complex peptide sequences. This compound is also beneficial in the study of protein interactions and the design of novel biomolecules, making it a crucial component in the toolkit of researchers focused on drug discovery and development.

Synonyms
( Acide S -Fmoc-2-amino-4-(3,4-diméthoxyphényl)-butyrique
CAS Number
1260616-59-8
Purity
≥ 98 % (HPLC)
Molecular Formula
C 27 H 276
Molecular Weight
461.51
MDL Number
MFCD07372404
PubChem ID
138108469
Appearance
Poudre blanche
Optical Rotation
[a] D 20 = -8 ± 1º (C = 1 dans DMF)
Conditions
Conserver à 0-8 °C
General Information
Synonyms
( Acide S -Fmoc-2-amino-4-(3,4-diméthoxyphényl)-butyrique
CAS Number
1260616-59-8
Purity
≥ 98 % (HPLC)
Molecular Formula
C 27 H 276
Molecular Weight
461.51
MDL Number
MFCD07372404
PubChem ID
138108469
Appearance
Poudre blanche
Optical Rotation
[a] D 20 = -8 ± 1º (C = 1 dans DMF)
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fmoc-L-3,4-dimethoxy-homophenylalanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a building block in the synthesis of peptides, allowing researchers to create complex structures for various applications in drug development and biotechnology.
  • Drug Discovery: Its unique properties make it valuable in the design of novel pharmaceuticals, particularly in targeting specific biological pathways, enhancing the efficacy of drug candidates.
  • Bioconjugation: The compound can be used to create bioconjugates, linking peptides to other molecules such as antibodies or enzymes, which is essential in developing targeted therapies.
  • Research in Neuroscience: It plays a role in studying neuropeptides, helping researchers understand their functions and potential therapeutic applications in neurological disorders.
  • Custom Peptide Libraries: This chemical is instrumental in generating diverse peptide libraries for high-throughput screening, facilitating the discovery of new bioactive compounds.

Citations