Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
39344
CAS Number:
2797-51-5
2-Amino-3-chloro-1,4-naphthoquinone
Purity:
≥ 98% (HPLC)
Synonym(s):
Quinoclamine
Documents
$73.71 /25G
Pack Size Availability Price
Request Bulk Quote
Product Information

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.

Synonyms
Quinoclamine
CAS Number
2797-51-5
Purity
≥ 98% (HPLC)
Molecular Formula
C10H6ClNO2
Molecular Weight
207.61
MDL Number
MFCD00001680
PubChem ID
17748
Melting Point
199 - 203 °C
Appearance
Orange, amber or dark red crystalline powder
Conditions
Store at RT
General Information
Synonyms
Quinoclamine
CAS Number
2797-51-5
Purity
≥ 98% (HPLC)
Molecular Formula
C10H6ClNO2
Molecular Weight
207.61
MDL Number
MFCD00001680
PubChem ID
17748
Melting Point
199 - 203 °C
Appearance
Orange, amber or dark red crystalline powder
Conditions
Store at RT
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
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