79010-36-9

Upstream product

• 25743-56-0 4-(1-oxopropyl)phenyl acetate 
• 79-03-8 propionyl chloride 
• 118-93-4 o-hydroxyacetophenone 

Downstream Products

• 79010-28-9 N-<β-(2-Acetyl-4-propionylphenoxy)ethyl>pyrrolidine 
• 141070-41-9 (E)-1-(2-Hydroxy-5-propionyl-phenyl)-3-p-tolyl-propenone 
• 141070-42-0 (E)-3-(4-Chloro-phenyl)-1-(2-hydroxy-5-propionyl-phenyl)-propenone 
• 79010-16-5 1,3-Bis(2'-acetyl-4'-propionylphenoxy)-2-propanol 
• 87544-99-8 (E)-1-(2-Hydroxy-5-propionyl-phenyl)-3-phenyl-propenone 
• 79010-35-8 1-(2'-Acetyl-4'-propionylphenoxy)-3-chloropropane 
• 131136-61-3 6-propionylflavonol 
• 131136-62-4 2-(4-methoxyphenyl)-3-methoxy-6-propionylchromone 
• 141070-46-4 3-Methoxy-2-phenyl-6-propionyl-chromen-4-one 
• 141070-47-5 3-Methoxy-6-propionyl-2-p-tolyl-chromen-4-one 
• 141070-62-4 2-(3-Methoxy-4-oxo-2-phenyl-4H-chromen-6-yl)-propionic acid 
• 141070-48-6 2-(4-Chloro-phenyl)-3-methoxy-6-propionyl-chromen-4-one 
• 141070-45-3 2-(4-methoxyphenyl)-3-methoxy-6-propionylchromone 
• 141070-54-4 2-(3-Methoxy-4-oxo-2-phenyl-4H-chromen-6-yl)-propionic acid methyl ester 

Relevant academic research and scientific papers

Synthesis and anticomplementary activity of 2-(2-aryl-3-alkoxychromon-6-yl)propanoic acids

The title compounds have been synthesized from the corresponding 2-aryl-3-alkoxy-6-propionylchromones by 1,2-migration of chromone ring using hypervalent iodine reagents.Seven selected compounds have been found to inhibit the in vitro immunohaemolysis of

1--3-substituted-aminopropanes and 2-Propanols as Potential Biodynamic Agents

2-Acetyl-4-(propionyl/bromo)phenols (3/4), prepared from 4-(propionyl/bromo)phenyl acetates (1/2), on alkylation with 1,3-dihalopropanes or epichlorohydrin gives the corresponding 3-halopropyl (5,6) and 2,3-epoxypropyl (7,8) ethers.Treatment of 5-8 with amines under suitable conditions yields the title compounds, 1-(2'-acetyl-4'-propionylphenoxy)-3-substituted-aminopropanes (9-11) and 1--3-substituted-amino-2-propanols (15-22).The corresponding β-pyrrolidinoethyl ethers (13,14) are prepared by alkylation of 3 and 4 with N-(β-chloroethyl)pyrrolidine.Dehydration of 10, 17 and 21 gives 12, 23 and 24, while reduction of 15 and 20 with KBH4 gives 25 and 26, respectively.Reaction of 3 and 4 with 0.5 mol of 1,3-dibromopropane and of 7 with 3 gives the corresponding 1,3-bis-aryloxypropanes (27,28) and 1,3-bis-aryloxy-2-propanol (29).Except 11 which exhibits antiinflammatory activity, no other compound shows any significant pharmacological activity.