227762-74-5

Upstream product

• 59443-15-1 5-chloro-3-bromo-2-hydroxyacetophenone 
• 100-52-7 benzaldehyde 
• 1224712-25-7 (E)-1-(3-bromo-5-chloro-2-hydroxyphenyl)-3-phenylprop-2-en-1-one 
• 174144-64-0 (E)-1-(3-Bromo-5-chloro-2-hydroxy-phenyl)-3-phenyl-propenone 

Downstream Products

• 910625-88-6 8-bromo-6-chloro-3-(ethoxycarbonylmethyloxy)flavone 
• 901768-89-6 8-benzyl-6-chloro-3-[3-(N-phthalimido)propoxy]flavone 
• 901768-92-1 8-benzyl-3-[3-(tert-butoxycarbonylamino)propoxy]-6-chloroflavone 
• 901768-84-1 8-allyl-6-chloro-3-hydroxyflavone 
• 901768-86-3 trifluoro-methanesulfonic acid 8-allyl-6-chloro-4-oxo-2-phenyl-4H-chromen-3-yl ester 
• 910625-97-7 6-chloro-3-hydroxy-8-(2-naphthyl)flavone 
• 909712-34-1 8-bromo-6-chloro-3-(trifluoromethylsulfonyloxy)flavone 
• 901768-88-5 8-bromo-6-chloro-3-[3-(N-phthalimido)propoxy]-flavone 

Relevant academic research and scientific papers

Synthesis of 2,3,6,8-tetrasubstituted chromone scaffolds

A useful and efficient synthetic strategy to 2,3,6,8-tetrasubstituted chromone derivatives has been developed. 2-Aryl/styryl-8-bromo-6-chloro-3- hydroxychromone derivatives were synthesized and used as scaffolds by introducing a variety of substituents in

A scaffold approach to 3,6,8-trisubstituted flavones

An efficient synthetic approach to 3,6,8-trisubstituted flavone scaffolds has been developed based on Pd-mediated coupling reactions. Georg Thieme Verlag Stuttgart.