79010-33-6

Basic information

• Product Name: 1-(2'-Acetyl-4'-propionylphenoxy)-2,3-epoxypropane
• CAS NO: 79010-33-6
• Molecular Weight: 248.279
• Mol File: 79010-33-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-(2'-Acetyl-4'-propionylphenoxy)-2,3-epoxypropane(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2'-Acetyl-4'-propionylphenoxy)-2,3-epoxypropane(79010-33-6)
• EPA Substance Registry System: 1-(2'-Acetyl-4'-propionylphenoxy)-2,3-epoxypropane(79010-33-6)

Safety Data

• Hazardous Substances Data: 79010-33-6(Hazardous Substances Data)

Upstream product

• 79010-36-9 2-Acetyl-4-propionylphenol 
• 106-89-8 epichlorohydrin 
• 25743-56-0 4-(1-oxopropyl)phenyl acetate 

Downstream Products

• 79010-24-5 1-{3-Acetyl-4-[2-hydroxy-3-(4-methyl-piperazin-1-yl)-propoxy]-phenyl}-propan-1-one 
• 79010-23-4 1-{3-Acetyl-4-[2-hydroxy-3-(4-phenyl-piperazin-1-yl)-propoxy]-phenyl}-propan-1-one 
• 79010-25-6 1-{3-Acetyl-4-[2-hydroxy-3-(4-hydroxy-4-phenyl-piperidin-1-yl)-propoxy]-phenyl}-propan-1-one 
• 79010-16-5 1,3-Bis(2'-acetyl-4'-propionylphenoxy)-2-propanol 
• 79030-60-7 1-(3-Acetyl-4-{3-[2-(3,4-dimethoxy-phenyl)-ethylamino]-2-hydroxy-propoxy}-phenyl)-propan-1-one 
• 79010-26-7 1-(2'-Acetyl-4'-propionylphenoxy)-3-isopropylamino-2-propanol 
• 79010-17-6 1-<2'-(α-Hydroxyethyl)-4'-(α-hydroxypropyl)phenoxy>-3-isopropylamino-2-propanol 
• 79010-19-8 1-{3-Acetyl-4-[2-hydroxy-3-(4-phenyl-3,6-dihydro-2H-pyridin-1-yl)-propoxy]-phenyl}-propan-1-one 

Relevant articles and documents

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.