953422-33-8

Basic information

• Product Name: 2-(4'-hydroxyphenyl)ethyl methyl carbonate
• Synonyms: 2-(4'-hydroxyphenyl)ethyl methyl carbonate
• CAS NO: 953422-33-8
• Molecular Weight: 196.203
• Mol File: 953422-33-8.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 2-(4'-hydroxyphenyl)ethyl methyl carbonate(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4'-hydroxyphenyl)ethyl methyl carbonate(953422-33-8)
• EPA Substance Registry System: 2-(4'-hydroxyphenyl)ethyl methyl carbonate(953422-33-8)

Safety Data

• Hazardous Substances Data: 953422-33-8(Hazardous Substances Data)

Upstream product

• 501-94-0 p-hydroxyphenethyl alcohol 
• 616-38-6 carbonic acid dimethyl ester 

Downstream Products

• 501-94-0 p-hydroxyphenethyl alcohol 
• 1552301-91-3 methyl [2-(2-oxo-4-(3,4,5-trimethoxyphenyl)chroman)-6-yl]ethyl carbonate 
• 1552302-00-7 3-(3,4-dimethoxyphenyl)-3-(2-hydroxy-5-(2-hydroxyethyl)phenyl)propanoic acid 
• 1552301-90-2 2-[4-(3,4-dimethoxyphenyl)-2-oxochroman-6-yl]ethyl methyl carbonate 
• 1552301-99-1 3-(2-hydroxy-5-(2-hydroxyethyl)phenyl)-3-(4-methoxyphenyl)propanoic acid 
• 1552301-89-9 2-[4-(4-methoxyphenyl)-2-oxochroman-6-yl]ethyl methyl carbonate 
• 85903-51-1 6,8-dimethyl-4-(4'-methoxyphenyl)-3,4-dihydrocoumarin 
• 1552301-97-9 methyl 3-(4-hydroxy-3,5-dimethylphenyl)-3-(4-methoxyphenyl)propanoate 
• 1552302-05-2 3-(4-hydroxy-3,5-dimethoxyphenyl)-3-(2-hydroxy-5-(2-hydroxyethyl)phenyl)propanoic acid 
• 1552301-95-7 2-[4-(4-hydroxy-3,5-dimethoxyphenyl)-2-oxochroman-6-yl]ethyl methyl carbonate 
• 1552301-94-6 2-[4-(3,4-dihydroxyphenyl)-2-oxochroman-6-yl]ethyl methyl carbonate 
• 1552302-03-0 3-(4-hydroxy-3-methoxyphenyl)-3-(2-hydroxy-5-(2-hydroxyethyl)phenyl)propanoic acid 
• 1552301-93-5 2-[4-(4-hydroxy-3-methoxyphenyl)-2-oxochroman-6-yl]ethyl methyl carbonate 
• 1552302-02-9 3-(2-hydroxy-5-(2-hydroxyethyl)phenyl)-3-(4-hydroxyphenyl)propanoic acid 

Relevant articles and documents

Chemoselective and efficient carbomethoxylation of the alcoholic chain of phenols by dimethyl carbonate (DMC)

The efficiency of dimethyl carbonate (DMC) as chemoselective carbomethoxylating agent of the alcoholic chain of phenols has been investigated. In the presence of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) or sulfuric acid as catalysts, new carbomethoxylated

Easy eco-friendly phenonium ion production from phenethyl alcohols in dimethyl carbonate

An efficient and simple one-pot procedure for selective etherification of 2-aryl-ethylalcohols has been achieved through Amberlyst 15-catalyzed reaction in dimethyl carbonate (DMC). Moreover, the polymer catalyst could be recovered and reused with no effect on its activity. The reaction mechanism involves the formation of phenonium ion which has been demonstrated by a C-C bond forming reaction. Theoretical studies are in agreement with and thus explain experimental results.

A singlet oxygen approach to oxaspirocycles

A method for the preparation of oxygen containing spirocycles using singlet oxygen is reported. A series of phenols were converted into the corresponding peroxy-cyclohexadienone derivatives by irradiation with visible light in the presence of a sensitizer and oxygen. The resulting peroxides could be converted into ether and lactone spirocycles in one or two steps. The synthesis of the oxaspirocycles from the phenols can also be performed in a one-pot fashion, avoiding the isolation of the peroxide intermediates.