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Catalog Number:
15679
CAS Number:
501015-36-7
Fmoc-(S-3-amino-3-(2,3-dimethoxyphenyl)propionic acid
Synonym(s):
Fmoc-L-β-Phe(2,3-dimethoxy)-OH, (S-Fmoc-2,3-dimethoxy-β-phenylalanine
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Product Information

Fmoc-(S)-3-amino-3-(2,3-dimethoxyphenyl)propionic acid is a versatile building block widely utilized in peptide synthesis and medicinal chemistry. 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 a 2,3-dimethoxyphenyl moiety, enhances its reactivity and compatibility with various coupling reagents, making it an ideal choice for researchers focused on developing complex peptide sequences.

In practical applications, Fmoc-(S)-3-amino-3-(2,3-dimethoxyphenyl)propionic acid is particularly valuable in the pharmaceutical industry for the design of bioactive peptides and drug candidates. Its ability to facilitate the synthesis of peptides with specific biological activities opens avenues for therapeutic development, including targeted drug delivery and the creation of novel therapeutics. Researchers appreciate its reliability and efficiency in peptide synthesis, which can significantly streamline their workflows and enhance the overall yield of desired products.

Synonyms
Fmoc-L-β-Phe(2,3-dimethoxy)-OH, (S-Fmoc-2,3-dimethoxy-β-phenylalanine
CAS Number
501015-36-7
Molecular Formula
C26H25NO6
Molecular Weight
447.49
MDL Number
MFCD03427982
PubChem ID
22309349
Conditions
Store at 0-8°C
General Information
Synonyms
Fmoc-L-β-Phe(2,3-dimethoxy)-OH, (S-Fmoc-2,3-dimethoxy-β-phenylalanine
CAS Number
501015-36-7
Molecular Formula
C26H25NO6
Molecular Weight
447.49
MDL Number
MFCD03427982
PubChem ID
22309349
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-(S)-3-amino-3-(2,3-dimethoxyphenyl)propionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in solid-phase peptide synthesis, allowing researchers to create complex peptides with high purity and yield.
  • Drug Development: It is used in the design of novel pharmaceuticals, particularly in developing compounds that target specific biological pathways, enhancing therapeutic efficacy.
  • Bioconjugation: The compound facilitates the attachment of biomolecules, such as proteins or nucleic acids, to surfaces or other molecules, which is crucial in creating targeted drug delivery systems.
  • Analytical Chemistry: It acts as a standard in various analytical techniques, helping researchers to calibrate instruments and validate methods for quantifying similar compounds.
  • Material Science: This chemical is employed in the development of functional materials, such as sensors or catalysts, due to its unique structural properties that enhance material performance.

Citations