27822-68-0 Usage
Description
1-(2-HydroxyMethyl-pyrrolidin-1-yl)-ethanone, also known as N-(2-Hydroxyethyl)-2-pyrrolidinone, is a cyclic amide with a pyrrolidinone ring and a hydroxyethyl group. It has the molecular formula C7H13NO2 and is commonly used as a solvent and a chemical intermediate in organic synthesis. 1-(2-HydroxyMethyl-pyrrolidin-1-yl)-ethanone is known for its high solvency power and its ability to dissolve a wide range of materials.
Uses
Used in Paint Industry:
1-(2-HydroxyMethyl-pyrrolidin-1-yl)-ethanone is used as a solubilizer and coupling agent for enhancing the solubility and stability of various components in paint formulations.
Used in Ink Industry:
In the ink industry, 1-(2-HydroxyMethyl-pyrrolidin-1-yl)-ethanone serves as a solubilizer and wetting agent, improving the flow and dispersion of ink on different surfaces.
Used in Adhesive Industry:
As a component in adhesive formulations, 1-(2-HydroxyMethyl-pyrrolidin-1-yl)-ethanone acts as a solubilizer and coupling agent, promoting better adhesion and compatibility with various substrates.
Used in Polymer Industry:
In polymer applications, 1-(2-HydroxyMethyl-pyrrolidin-1-yl)-ethanone is utilized as a solubilizer and wetting agent, contributing to the improved processability and performance of polymer materials.
Used in Organic Synthesis:
1-(2-HydroxyMethyl-pyrrolidin-1-yl)-ethanone is employed as a reaction medium in organic synthesis due to its high boiling point and low vapor pressure, making it an ideal solvent for a variety of chemical reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 27822-68-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,8,2 and 2 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 27822-68:
(7*2)+(6*7)+(5*8)+(4*2)+(3*2)+(2*6)+(1*8)=130
130 % 10 = 0
So 27822-68-0 is a valid CAS Registry Number.
27822-68-0Relevant articles and documents
Additive-free chemoselective acylation of amines
Temperini, Andrea,Terlizzi, Raffaella,Testaferri, Lorenzo,Tiecco, Marcello
experimental part, p. 295 - 302 (2010/03/30)
Aliphatic and aromatic amines are efficiently acylated by acetic, pivalic, benzoic, phthalic, or maleic anhydrides in ethyl acetate at room temperature. Under the same experimental conditions, amino alcohols are chemoselectively acylated at the amino group.
Synthesis of Analogues of 1,3-Dihydroxyacetone Phosphate and Glyceraldehyde 3-Phosphate for Use in Studies of Fructose-1,6-diphosphate Aldolase
Bischofberger, Norbert,Waldmann, Herbert,Saito, Tohru,Simon, Ethan S.,Lees, Watson,et al.
, p. 3457 - 3465 (2007/10/02)
This paper describes the synthesis of five analogues of dihydroxyacetone phosphate (3-azidohydroxyacetone 1-phosphate (5), 3-(acetylamino)hydroxyacetone 1-phosphate (12), (R)-1,3-dihydroxy-2-butanone 1-phosphate (18), (+/-)-1,3-dihydroxy-2-butanone 3-phosphate (26), and phosphonomethyl glycolate (31)).The syntheses of 18 and 26 are based on a new reaction: that is, the introduction of the phosphate group by the reaction of a diazo ketone with dibenzyl phosphate.These methods provide easy access to a number of compounds that are potential substrates for the synthetically useful enzyme aldolase (fructose-1,6-diphosphate aldolase from rabbit muscle, EC 4.1.2.13, RAMA) and perhaps for other enzymes of glycolysis.This paper also describes syntheses of 14 aldehydes for examination as substrates for aldolase.When the precursor was available, ozonolysis of vinyl groups proved to be the best route to the corresponding aldehydes.
