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Catalog Number:
29652
CAS Number:
256935-69-0
Acide Fmoc-3-amino-4-méthoxy-benzoïque
Purity:
≥ 99 % (HPLC)
Documents
$127.79 /1G
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Product Information

Fmoc-3-amino-4-methoxy-benzoic acid 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 efficient coupling reactions, making it an invaluable tool for researchers in the fields of medicinal chemistry and biochemistry. The methoxy groups enhance its solubility and reactivity, facilitating smoother reactions and higher yields in peptide synthesis.

In addition to its role in peptide synthesis, Fmoc-3-amino-4-methoxy-benzoic acid has potential applications in the development of pharmaceuticals and biologically active compounds. Its ability to serve as a building block for more complex molecules opens avenues for the design of targeted therapies. Researchers appreciate its stability and compatibility with various coupling reagents, which streamline the synthesis process. Overall, this compound stands out for its practical applications in research and industry, making it a preferred choice for professionals seeking reliable and efficient solutions in their work.

CAS Number
256935-69-0
Purity
≥ 99 % (HPLC)
Molecular Formula
C 23 H 195
Molecular Weight
389.41
MDL Number
MFCD02682216
PubChem ID
10916111
Appearance
Poudre blanche
Conditions
Conserver à 0-8 °C
General Information
CAS Number
256935-69-0
Purity
≥ 99 % (HPLC)
Molecular Formula
C 23 H 195
Molecular Weight
389.41
MDL Number
MFCD02682216
PubChem ID
10916111
Appearance
Poudre blanche
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fmoc-3-amino-4-methoxy-benzoic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in peptide synthesis, allowing for selective reactions and enhancing the yield of desired peptides.
  • Drug Development: Its unique structure aids in the design of novel pharmaceuticals, particularly in creating compounds with improved bioavailability and efficacy.
  • Bioconjugation: It is used in bioconjugation processes, facilitating the attachment of biomolecules to surfaces or other molecules, which is crucial in developing targeted drug delivery systems.
  • Research in Material Science: The compound contributes to the development of advanced materials, such as polymers and nanomaterials, by modifying their properties for specific applications.
  • Diagnostic Applications: Its role in creating biosensors and diagnostic tools enhances the detection of biomolecules, improving the accuracy and speed of medical diagnostics.

Citations