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Catalog Number:
39344
CAS Number:
2797-51-5
2-Amino-3-chloro-1,4-naphtoquinone
Purity:
≥ 98 % (HPLC)
Synonym(s):
Quinoclamine
Documents
$73.71 /25G
Taille
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Informations sur le produit

2-Amino-3-chloro-1,4-naphthoquinone is a versatile compound known for its significant applications in various fields, particularly in organic synthesis and medicinal chemistry. This compound exhibits unique properties that make it valuable for researchers and industry professionals alike. Its ability to act as a precursor in the synthesis of complex organic molecules allows for the development of novel pharmaceuticals and agrochemicals. Additionally, its chlorinated structure enhances its reactivity, making it an effective intermediate in dye production and other chemical processes.

In the realm of medicinal chemistry, 2-Amino-3-chloro-1,4-naphthoquinone has shown potential as an antitumor agent, with studies indicating its efficacy against certain cancer cell lines. Its application in the development of photodynamic therapy agents also highlights its relevance in advanced therapeutic strategies. With its unique chemical properties and diverse applications, this compound stands out as a crucial building block for innovative research and industrial processes.

Numéro CAS 
2797-51-5
Formule moléculaire
C10H6ClNO2
Poids moléculaire 
207.61
Point de fusion 
199 - 203 °C
Informations générales
Numéro CAS 
2797-51-5
Formule moléculaire
C10H6ClNO2
Poids moléculaire 
207.61
Point de fusion 
199 - 203 °C
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
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Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

2-Amino-3-chloro-1,4-naphthoquinone is widely utilized in research focused on:

  • Pharmaceutical Development: This compound is a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of anti-cancer agents due to its ability to inhibit certain enzymes involved in tumor growth.
  • Dyes and Pigments: Its vibrant color properties make it useful in the production of dyes and pigments for textiles and inks, providing a stable and long-lasting color that is resistant to fading.
  • Biochemical Research: The compound serves as a valuable reagent in biochemical assays, particularly in studies involving oxidative stress and cellular signaling pathways, helping researchers understand disease mechanisms.
  • Electrochemical Applications: It is used in the development of electrochemical sensors, where its redox properties allow for the detection of various analytes, enhancing the sensitivity and specificity of the sensors.
  • Environmental Monitoring: This chemical can be employed in environmental studies to detect and quantify pollutants, contributing to efforts in assessing and mitigating environmental contamination.

Citations