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Catalog Number:
07335
CAS Number:
184962-88-7
Fmoc-3,4-dimetoxi-L-fenilalanina
Purity:
≥ 99 % (HPLC)
Synonym(s):
Fmoc-L-Phe(3,4-Dimetoxi)-OH, Fmoc-3,4-dimetoxi-L-Phe-OH, Ácido ( S -Fmoc-2-amino-3-(3,4-dimetoxifenil)propiónico
Documents
$60.40 /100 mg
Tamaño
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Product Information

Fmoc-3,4-dimethoxy-L-phenylalanine 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 solid-phase peptide synthesis. Its unique structure, characterized by the presence of two methoxy groups on the phenyl ring, enhances its reactivity and solubility, making it an excellent choice for researchers looking to create complex peptides with high purity and yield.

In the pharmaceutical industry, Fmoc-3,4-dimethoxy-L-phenylalanine serves as a crucial building block for the synthesis of bioactive peptides and therapeutic agents. Its application extends to the development of peptide-based drugs, where it contributes to the stability and efficacy of the final product. Researchers appreciate its ability to facilitate the synthesis of peptides with specific biological activities, thereby accelerating the discovery of new therapeutic compounds. With its favorable properties and practical applications, this compound is an invaluable asset for professionals in the fields of medicinal chemistry and biochemistry.

Synonyms
Fmoc-L-Phe(3,4-Dimetoxi)-OH, Fmoc-3,4-dimetoxi-L-Phe-OH, Ácido ( S -Fmoc-2-amino-3-(3,4-dimetoxifenil)propiónico
CAS Number
184962-88-7
Purity
≥ 99 % (HPLC)
Molecular Formula
C26H25NO6
Molecular Weight
447.5
MDL Number
MFCD01317730
PubChem ID
4712577
Appearance
Polvo blanco
Optical Rotation
[a] D 20 = -26 ± 2 º (C=1 en DMF)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-L-Phe(3,4-Dimetoxi)-OH, Fmoc-3,4-dimetoxi-L-Phe-OH, Ácido ( S -Fmoc-2-amino-3-(3,4-dimetoxifenil)propiónico
CAS Number
184962-88-7
Purity
≥ 99 % (HPLC)
Molecular Formula
C26H25NO6
Molecular Weight
447.5
MDL Number
MFCD01317730
PubChem ID
4712577
Appearance
Polvo blanco
Optical Rotation
[a] D 20 = -26 ± 2 º (C=1 en DMF)
Conditions
Conservar entre 0 y 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-3,4-dimethoxy-L-phenylalanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a building block in solid-phase peptide synthesis, allowing researchers to create complex peptides efficiently.
  • Drug Development: It is used in the design of peptide-based drugs, particularly in targeting specific biological pathways, enhancing therapeutic efficacy.
  • Bioconjugation: The chemical's unique structure facilitates bioconjugation processes, enabling the attachment of peptides to various biomolecules for targeted delivery systems.
  • Analytical Chemistry: It acts as a standard in analytical methods for characterizing peptides, ensuring accuracy in research and quality control.
  • Research in Neuroscience: This compound is instrumental in studying neuropeptides, contributing to advancements in understanding neurological disorders and developing potential treatments.

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