146463-87-8

Upstream product

• 541-41-3 chloroformic acid ethyl ester 
• 103814-48-8 N-(3-((tetrahydro-2H-pyran-2-yl)oxy)phenyl)pivalamide 

Downstream Products

• 130600-46-3 2,2-Dimethyl-N-[2-{3-oxo-3-[4-(tetrahydro-pyran-2-yloxy)-phenyl]-propionyl}-3-(tetrahydro-pyran-2-yloxy)-phenyl]-propionamide 
• 130600-02-1 2,2-Dimethyl-N-[2-[3-(4-methylamino-phenyl)-3-oxo-propionyl]-3-(tetrahydro-pyran-2-yloxy)-phenyl]-propionamide 
• 130600-56-5 N-[2-[3-(4-Bromo-phenyl)-3-oxo-propionyl]-3-(tetrahydro-pyran-2-yloxy)-phenyl]-2,2-dimethyl-propionamide 
• 130599-99-4 N-[2-{3-[3-(2,2-Dimethyl-propionylamino)-phenyl]-3-oxo-propionyl}-3-(tetrahydro-pyran-2-yloxy)-phenyl]-2,2-dimethyl-propionamide 
• 130599-97-2 N-[2-{3-[4-(2,2-Dimethyl-propionylamino)-phenyl]-3-oxo-propionyl}-3-(tetrahydro-pyran-2-yloxy)-phenyl]-2,2-dimethyl-propionamide 
• 130600-12-3 N-[2-{3-[4-(Acetyl-ethyl-amino)-phenyl]-3-oxo-propionyl}-3-(tetrahydro-pyran-2-yloxy)-phenyl]-2,2-dimethyl-propionamide 
• 130600-19-0 N-[2-{3-[4-(Acetyl-propyl-amino)-phenyl]-3-oxo-propionyl}-3-(tetrahydro-pyran-2-yloxy)-phenyl]-2,2-dimethyl-propionamide 
• 130600-42-9 N-[2-{3-[4-(Acetyl-methoxymethyl-amino)-phenyl]-3-oxo-propionyl}-3-(tetrahydro-pyran-2-yloxy)-phenyl]-2,2-dimethyl-propionamide 
• 130639-79-1 N-[2-{3-[4-(Acetyl-butyl-amino)-phenyl]-3-oxo-propionyl}-3-(tetrahydro-pyran-2-yloxy)-phenyl]-2,2-dimethyl-propionamide 
• 152169-36-3 ethyl 6-(N-ethoxycarbonylamino)-2-hydroxybenzoate 
• 152169-39-6 ethyl 6-(N-ethoxycarbonylamino)-3-fluoro-2-hydroxybenzoate 
• 152169-37-4 ethyl 2-(N-ethoxycarbonylamino)-3-fluoro-6-hydroxybenzoate 
• 152169-41-0 ethyl 3,5-difluoro-6-(N-ethoxycarbonylamino)-2-hydroxybenzoate 
• 152169-40-9 6-Ethoxycarbonylamino-3-fluoro-2-methoxymethoxy-benzoic acid ethyl ester 

Relevant academic research and scientific papers

Synthesis of a 6H-pyrazolo[4,5,1-de]acridin-6-one derivative: A useful intermediate of antitumour agents

A 6H-pyrazolo[4,5,1-de]acridin-6-one derivative, a useful intermediate of antitumor agents, was prepared by a facile synthetic route from 2-bromobenzoic acid and 6-nitroindazole involving a halogenocopper(I)-catalyzed Ullmann coupling reaction and Friedel-Crafts cyclization.

5-aminoflavone derivatives

5-Aminoflavone derivatives represented by the formula (I): STR1 wherein R1, R2, R3 and R4 are the same or different and represent hydrogen, substituted or unsubstituted lower alkyl, lower alkenyl, halogen-substi