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Catalog Number:
32745
CAS Number:
396717-86-5
N-(4-méthoxyphénylazoformyl)-Phe-OH·sel de potassium
Purity:
≥ 96 % (HPLC)
Synonym(s):
L'AFP
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$160.00 /5 mg
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Product Information

N-(4-Methoxyphenylazoformyl)-Phe-OH·potassium salt is a versatile compound with significant applications in the fields of biochemistry and pharmaceuticals. This potassium salt derivative is recognized for its unique azo group, which enhances its reactivity and solubility, making it an ideal candidate for various research applications. Its structure allows for effective binding in biochemical assays, particularly in the study of enzyme interactions and protein-ligand binding. Researchers have utilized this compound in the development of novel therapeutic agents, showcasing its potential in drug formulation and delivery systems.

In addition to its research applications, N-(4-Methoxyphenylazoformyl)-Phe-OH·potassium salt serves as a valuable tool in the synthesis of complex organic molecules. Its ability to facilitate reactions in a controlled manner makes it advantageous for chemists looking to streamline their synthetic pathways. The compound's stability and compatibility with various solvents further enhance its utility in laboratory settings, providing researchers with a reliable option for their experimental needs. Overall, this compound stands out for its practical applications in both academic and industrial research, offering a promising avenue for innovation in chemical synthesis and drug development.

Synonyms
L'AFP
CAS Number
396717-86-5
Purity
≥ 96 % (HPLC)
Molecular Formula
C17H16KN3O4
Molecular Weight
365.43
MDL Number
MFCD01318845
PubChem ID
139211134
Appearance
Poudre amorphe de couleur orange
Conditions
Conserver à - 20 °C
General Information
Synonyms
L'AFP
CAS Number
396717-86-5
Purity
≥ 96 % (HPLC)
Molecular Formula
C17H16KN3O4
Molecular Weight
365.43
MDL Number
MFCD01318845
PubChem ID
139211134
Appearance
Poudre amorphe de couleur orange
Conditions
Conserver à - 20 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

N-(4-Methoxyphenylazoformyl)-Phe-OH·potassium salt is widely utilized in research focused on:

  • Biochemical Research: This compound serves as a valuable reagent in the synthesis of peptide-based drugs, aiding researchers in developing new therapeutic agents.
  • Colorimetric Assays: Its azo group allows for colorimetric detection in various assays, making it useful in laboratories for quantifying biomolecules.
  • Analytical Chemistry: Employed in chromatography, it helps in separating and identifying complex mixtures, enhancing the accuracy of analytical results.
  • Pharmaceutical Development: The compound's properties facilitate the formulation of innovative drug delivery systems, improving the bioavailability of active ingredients.
  • Material Science: It is used in the development of smart materials that respond to environmental stimuli, showcasing its versatility beyond traditional applications.

Citations