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Catalog Number:
15045
CAS Number:
120467-46-1
Ácido Fmoc- N -metil-2-aminobenzoico
Purity:
≥ 99 % (HPLC)
Synonym(s):
Ácido Fmoc- N -metil-antranílico, Fmoc- N -Me-2-Abz-OH
Documents
$134.70 /1G
Tamaño
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Información del producto

Fmoc-N-methyl-2-aminobenzoic acid is a versatile building block widely utilized in peptide synthesis and drug development. This compound, known for its protective Fmoc (9-fluorenylmethoxycarbonyl) group, facilitates the selective modification of amino acids, making it an essential reagent in solid-phase peptide synthesis. Its unique structure allows for enhanced stability and solubility, which are critical in various organic synthesis applications. Researchers appreciate its ability to streamline the synthesis process, thereby improving yields and reducing reaction times.

In addition to its role in peptide synthesis, Fmoc-N-methyl-2-aminobenzoic acid is also valuable in the development of pharmaceuticals and biologically active compounds. Its application extends to the creation of targeted drug delivery systems and the exploration of new therapeutic agents. The compound's compatibility with various coupling reagents and its ease of removal under mild conditions make it a preferred choice among chemists and researchers. Overall, Fmoc-N-methyl-2-aminobenzoic acid stands out for its efficiency and effectiveness in advancing chemical research and development.

Número CAS
120467-46-1
Fórmula molecular
C 23 H 19 N.º 4
Peso molecular
373.41
Número MDL
MFCD04972602
Punto de fusión
132-142 °C
Condiciones
Conservar entre 0 y 8 °C.
Información general
Número CAS
120467-46-1
Fórmula molecular
C 23 H 19 N.º 4
Peso molecular
373.41
Número MDL
MFCD04972602
Punto de fusión
132-142 °C
Condiciones
Conservar entre 0 y 8 °C.
Propiedades
¡Pronto habrá más información sobre la propiedad!
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Seguridad y normativas
Materiales peligrosos
-
Antibiótico
-
Regulado por la DEA
No
Advertencias
-
Aplicaciones

Fmoc-N-methyl-2-aminobenzoic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in solid-phase peptide synthesis, allowing for the selective modification of amino acids without interfering with other functional groups.
  • Drug Development: It is used in the design of peptide-based drugs, particularly in the pharmaceutical industry, where its ability to enhance stability and bioavailability is crucial.
  • Bioconjugation: Researchers employ this chemical in bioconjugation processes, facilitating the attachment of biomolecules to surfaces or other molecules, which is essential in creating targeted therapies.
  • Analytical Chemistry: It aids in the development of analytical methods for detecting and quantifying peptides, improving the accuracy and efficiency of biochemical assays.
  • Material Science: The compound is also explored in the development of new materials, particularly in creating functionalized surfaces that can interact with biological systems.

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