7495-50-3

Usage

Chemical compound

6-chloro-4-(4-chlorophenyl)naphtho[2,3-c]furan-1,3-dione
Naphthalene core containing two chlorine atoms and a furan ring
Commonly used as a reagent in organic synthesis
Potential applications in pharmaceuticals and agrochemicals
Biological activities include anti-inflammatory, anti-cancer, and anti-microbial properties
Versatile building block for the synthesis of diverse organic compounds
Valuable in scientific research and chemical manufacturing
Potential therapeutic uses make it an important target for further study and development.

Upstream product

• 24654-08-8 3-(2-chlorophenyl)prop-2-ynoic acid 
• 42122-34-9 3-(4-chlorophenyl)propioloyl chloride 
• 131361-75-6 bis-((E)-4-chloro-benzylidene)-succinic acid-anhydride 
• 7553-56-2 iodine 
• 3240-10-6 (4-chlorophenyl)propiolic acid 
• 471-25-0 Propiolic acid 

Downstream Products

• 7495-49-0 2,9-dichloro-7-oxo-7H-benzo[c]fluorene-6-carboxylic acid 

Relevant academic research and scientific papers

One-pot syntheses of blue-luminescent 4-aryl-1H-benzo[f]isoindole-1, 3(2H)-diones by T3P activation of 3-arylpropiolic acids

In situ activation of 3-arylpropiolic acids with T3P (n-propylphosphonic acid anhydride) initiates a domino reaction furnishing 4-arylnaphtho[2, 3-c]furan-1, 3-diones in excellent yields. Upon employing these anhydrides as reactive intermediates blue-lumi

Room temperature cyclization of arylpropiolic acid anhydride: Synthesis of naphtho[2,3-c]furan-1,3-dione derivatives

Cyclic anhydrides such as naphtho[2,3-c]furan-1,3-dione derivatives were synthesized from the reaction of arylpropiolic acids and 2-chloro-4,6-dimethoxy-1,3,5-triazine in the presence of N-methylmorpholine at room temperature. This mild condition provided

Synthesis and fluorescence of the new environment-sensitive fluorophore 6-chloro-2,3-naphthalimide derivative

Convenient and efficient synthesis of a new environmentally sensitive chlorine-substituted 2,3-naphthalimide-based fluorophore is reported. Benzotriazole carboxyl group activation of the 6-chloro-fluorophore enabled quick labeling of free and Fmoc-protected amino acids. The photophysical properties of the compounds obtained include high quantum yields in solvents of different polarity: water, methanol, acetonitrile and hexane.