13932-53-1

Usage

Uses

Used in Pharmaceutical Industry:
Carbonic acid,esters,monoethyl ester is used as a solvent in the production of certain pharmaceuticals. Its ability to dissolve a wide range of compounds makes it suitable for use in the synthesis of drugs and other medicinal products.
Used in Organic Synthesis:
In the field of organic synthesis, carbonic acid,esters,monoethyl ester serves as a reagent. It is used in various chemical reactions to form new compounds, contributing to the development of new materials and products.
Used in Beverage Industry:
Carbonic acid,esters,monoethyl ester is used in the beverage industry, particularly in the production of fizzy drinks and soda water. Its ability to dissolve carbon dioxide contributes to the formation of carbonation, giving these beverages their characteristic effervescence.
Used in Carbon Dioxide Transport:
In the medical field, carbonic acid,esters,monoethyl ester plays a role in the transport of carbon dioxide in the bloodstream. Its presence helps facilitate the movement of this essential gas, maintaining the balance of acid-base in the body.

Upstream product

• 14666-78-5 Peroxydikohlensaeure-diethylester 
• 1500-76-1 3-Cyclohexylamino-5,5-dimethyl-2-cyclohexen-1-on 
• 80179-75-5 ethyl N-3,5-dinitrophenyl-N-methylcarbamate 
• 80179-76-6 ethyl N-methyl-N-4-nitrophenylcarbamate 

Downstream Products

• 102131-26-0 C₁₅H₁₈O₆ 
• 565-80-0 2,4-dimethylpentan-3-one 
• 1619-62-1 2,2-dimethylmalonic acid diethyl ester 
• 684287-67-0 carbonic acid 9-benzhydryloxy-7-(2,4-dimethoxy-benzyl)-6,8-dioxo-7,8-dihydro-6H-pyrrolo[3,4-g]quinolin-5-yl ester ethyl ester 
• 684287-77-2 carbonic acid 9-benzhydryloxy-7-[2-(4-fluoro-phenyl)-ethyl]-6,8-dioxo-7,8-dihydro-6H-pyrrolo[3,4-g]quinolin-5-yl ester ethyl ester 
• 189814-33-3 α-chloromethyl-2-methoxy-5-sulphamoylbenzenemethanol 
• 541-41-3 chloroformic acid ethyl ester 
• 55457-59-5 8-bromo-2,7-dimethyl-3H-pyrazolo[1,5-a][1,3,5]triazin-4-one 
• 1196969-15-9 C₂₅H₂₈N₂O₄ 
• 1196968-95-2 C₂₆H₂₉NO₄ 
• 1188392-64-4 1-(3'-hydroxyphenyl)-2-ethoxycarboxyl-6,7-dioxolo-1,2,3,4-tetrahydroisoquinoline 

Relevant academic research and scientific papers

Basic Hydrolysis of Some Alkyl and Phenyl N-Aryl-N-methylcarbamates.

Rate constants for the basic hydrolysis of methyl, ethyl and phenyl N-aryl-N-methylcarbamates in the presence and absence of micelles of cetyltrimethylammonium bromide are reported.Hammett plots for the methyl aand ethyl carbamates were curved, and this is explained by consideration of the competition between C-N and C-OR bond breaking for decomposition of the tetrahedral intermediate.In one case (p-nitro-substituted), rate-determining formation of the tetrahedral intermediate is suggested, whereas for other compounds rate-determining C-N bond breaking or C-OR bond bre aking is proposed.Micellar catalysis for each of the reactions is reported, and large catalysis (x 50) was observed for compounds where C-N bond breaking was kinetically significant.This is compared with results in the literature for amide and ester hydrolysis.Whereas, for ester hydrolysis, loss of alkoxide ion from the tetrahedral intermediate is favoured over loss of hydroxide ion, in carbamate hydrolysis, loss of hydroxide ions is favoured.A possible reason for this reversal of nucleofugicity of OH- and OR- is proposed.

Einfuehrung von Sauerstoff-Funktionen in die α-Stellung von β-Diketonen, 5. Acyloxylierung von 3-prim.-Amino-2-cyclohexen-1-onen

The enaminone 1 reacts with diacyl peroxides 2 to yield monoacyloxylation products 4 and (acylamino)cyclohexadienolones 6 which may be regarded as reaction products of an acyl rearrangement of the non-isolable bis-acyloxylation products 5.Catalytic hydrogenation of benzyl esters 4e and 6e obtained by the described way leads immediately to the amino reductone 8.