75200-57-6

Basic information

• Product Name: 7-acetoxy-4-methyl-3-phenyl-2H-1-benzopyran-2-one
• CAS NO: 75200-57-6
• Molecular Weight: 294.307
• Mol File: 75200-57-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 7-acetoxy-4-methyl-3-phenyl-2H-1-benzopyran-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: 7-acetoxy-4-methyl-3-phenyl-2H-1-benzopyran-2-one(75200-57-6)
• EPA Substance Registry System: 7-acetoxy-4-methyl-3-phenyl-2H-1-benzopyran-2-one(75200-57-6)

Safety Data

• Hazardous Substances Data: 75200-57-6(Hazardous Substances Data)

Upstream product

• 108-24-7 acetic anhydride 
• 103-82-2 phenylacetic acid 
• 89-84-9 2',4'-dihydroxy-4-acetophenone 
• 114-70-5 sodium phenylacetate 

Downstream Products

• 873403-43-1 6,8-dibromo-7-hydroxy-4-methyl-3-phenyl-coumarin 
• 212694-37-6 6-bromo-7-hydroxy-4-methyl-3-phenyl-coumarin 
• 672938-11-3 8-bromo-7-hydroxy-4-methyl-3-phenyl-coumarin 
• 23028-24-2 7-methoxy-4-methyl-3-phenylcoumarin 
• 75200-67-8 5-Methyl-3-[4-(2-morpholin-4-yl-ethoxy)-phenyl]-2,6-diphenyl-furo[3,2-g]chromen-7-one 
• 75200-70-3 5-Methyl-2,6-diphenyl-3-[4-(2-piperazin-1-yl-ethoxy)-phenyl]-furo[3,2-g]chromen-7-one 
• 75200-63-4 5-Methyl-2,6-diphenyl-3-[4-(3-piperidin-1-yl-propoxy)-phenyl]-furo[3,2-g]chromen-7-one 
• 75200-68-9 5-Methyl-2,6-diphenyl-3-[4-(2-piperidin-1-yl-ethoxy)-phenyl]-furo[3,2-g]chromen-7-one 
• 75200-69-0 5-Methyl-2,6-diphenyl-3-[4-(2-pyrrolidin-1-yl-ethoxy)-phenyl]-furo[3,2-g]chromen-7-one 
• 75200-65-6 3-[4-(2-Diethylamino-ethoxy)-phenyl]-5-methyl-2,6-diphenyl-furo[3,2-g]chromen-7-one 
• 75200-66-7 3-[4-(2-Dimethylamino-ethoxy)-phenyl]-5-methyl-2,6-diphenyl-furo[3,2-g]chromen-7-one 
• 75200-61-2 2,6-Diphenyl-3-(p-methoxyphenyl)-5-methyl-7-oxo-7H-furo<3,2-g><1>benzopyran 
• 75200-60-1 7-(1'-Phenyl-2'-p-methoxyphenyl-2'-oxo)-ethyloxy-4-methyl-3-phenylcoumarin 
• 75200-62-3 2,6-Diphenyl-3-(p-hydroxyphenyl)-5-methyl-7-oxo-7H-furo<3,2-g><1>benzopyran 

Relevant articles and documents

One-pot greener protocol for the synthesis of substituted coumarins

An expeditious one-pot procedure for the synthesis of substituted coumarins under microwave irradiation is accounted. The method describes an easy and fast method for the synthesis of substituted acetoxy coumarins which are very good fluorophores for medical as well as industrial applications. It makes use of easily available reagents such as triethylamine and acetic anhydride as catalyst. The method finds good applications for the synthesis of multisubstituted coumarins.

Synthesis of 2,6-Diphenyl-3-(p-substituted phenyl)-5-methyl-7-oxo-7H-furobenzopyrans

Some 2,6-diphenyl-3-(p-alkylaminoalkoxy)phenyl-5-methyl-7-oxo-7H-furobenzopyrans (Ib-i) have been synthesized.All the compounds are found to be devoid of anti-implantation activity at a dose level of 25 mg/kg/day, when tested on albino rats.