Category: 62020-09-1

Blades, Kevin et al. published their research in Tetrahedron Letters in 2014 | CAS: 62020-09-1

Methyl 2-(methylsulfonyl)acetate (cas: 62020-09-1) belongs to esters. Esters are also usually derived from carboxylic acids. It may also be obtained by reaction of acid anhydride or acid halides with alcohols or by the reaction of salts of carboxylic acids with alkyl halides. Esters contain a carbonyl center, which gives rise to 120° C–C–O and O–C–O angles. Unlike amides, esters are structurally flexible functional groups because rotation about the C–O–C bonds has a low barrier. Their flexibility and low polarity is manifested in their physical properties; they tend to be less rigid (lower melting point) and more volatile (lower boiling point) than the corresponding amides. Safety of Methyl 2-(methylsulfonyl)acetate

Expedient synthesis of biologically important sulfonylmethyl pyrimidines was written by Blades, Kevin;Demeritt, Julie;Fillery, Shaun;Foote, Kevin M.;Greenwood, Ryan;Gregson, Clare;Hassall, Lorraine A.;McGuire, Thomas M.;Pike, Kurt G.;Williams, Emma. And the article was included in Tetrahedron Letters in 2014.Safety of Methyl 2-(methylsulfonyl)acetate This article mentions the following:

Two novel synthetic strategies that allow rapid diversification of the sulfone moiety in sulfonylmethyl pyrimidines, a class of compounds with a wide range of biol. activity, which are of interest in a wide variety of drug discovery programs, are described. In the experiment, the researchers used many compounds, for example, Methyl 2-(methylsulfonyl)acetate (cas: 62020-09-1Safety of Methyl 2-(methylsulfonyl)acetate).

Methyl 2-(methylsulfonyl)acetate (cas: 62020-09-1) belongs to esters. Esters are also usually derived from carboxylic acids. It may also be obtained by reaction of acid anhydride or acid halides with alcohols or by the reaction of salts of carboxylic acids with alkyl halides. Esters contain a carbonyl center, which gives rise to 120° C–C–O and O–C–O angles. Unlike amides, esters are structurally flexible functional groups because rotation about the C–O–C bonds has a low barrier. Their flexibility and low polarity is manifested in their physical properties; they tend to be less rigid (lower melting point) and more volatile (lower boiling point) than the corresponding amides. Safety of Methyl 2-(methylsulfonyl)acetate

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Gipstein, E. et al. published their research in Journal of Organic Chemistry in 1980 | CAS: 62020-09-1

Methyl 2-(methylsulfonyl)acetate (cas: 62020-09-1) belongs to esters. Volatile esters with characteristic odours are used in synthetic flavours, perfumes, and cosmetics. Certain volatile esters are used as solvents for lacquers, paints, and varnishes. Esters contain a carbonyl center, which gives rise to 120° C–C–O and O–C–O angles. Unlike amides, esters are structurally flexible functional groups because rotation about the C–O–C bonds has a low barrier. Their flexibility and low polarity is manifested in their physical properties; they tend to be less rigid (lower melting point) and more volatile (lower boiling point) than the corresponding amides. COA of Formula: C4H8O4S

Synthesis and polymerization of alkyl α-(Alkylsulfonyl)acrylates was written by Gipstein, E.;Willson, C. G.;Sachdev, H.. And the article was included in Journal of Organic Chemistry in 1980.COA of Formula: C4H8O4S This article mentions the following:

The reaction of RSO2CHMeCO2R1 (R = Me, CMe3; R1 = CMe3, Me) with PhSeCl gave RSO2C(SePh)MeCO2R1, the selenide products were treated with H2O2, and Se-oxidation was followed by an elimination reaction to yield the resp. RSO2C:(CH2)CO2R1 (I). The deacylative methylenation of MeSO2CH(COPh)CO2Me by HCHO gave I (R = R1 = Me). The I (R1 = Me) polymerized more readily than the I (R1 = CMe3). In the experiment, the researchers used many compounds, for example, Methyl 2-(methylsulfonyl)acetate (cas: 62020-09-1COA of Formula: C4H8O4S).

Methyl 2-(methylsulfonyl)acetate (cas: 62020-09-1) belongs to esters. Volatile esters with characteristic odours are used in synthetic flavours, perfumes, and cosmetics. Certain volatile esters are used as solvents for lacquers, paints, and varnishes. Esters contain a carbonyl center, which gives rise to 120° C–C–O and O–C–O angles. Unlike amides, esters are structurally flexible functional groups because rotation about the C–O–C bonds has a low barrier. Their flexibility and low polarity is manifested in their physical properties; they tend to be less rigid (lower melting point) and more volatile (lower boiling point) than the corresponding amides. COA of Formula: C4H8O4S

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics