409335-13-3 Usage
Uses
Used in Inks:
2-Pyrrolidinone,1-[(2R)-oxiranylmethyl]-(9CI) is used as a solvent in the ink industry for its ability to dissolve various pigments and dyes, ensuring consistent ink flow and performance.
Used in Coatings:
In the coatings industry, 2-Pyrrolidinone,1-[(2R)-oxiranylmethyl]-(9CI) is utilized as a solvent to enhance the solubility of resins and other components, contributing to improved coating properties such as adhesion, durability, and appearance.
Used in Adhesives:
2-Pyrrolidinone,1-[(2R)-oxiranylmethyl]-(9CI) is employed as a solvent in adhesive formulations to improve the adhesive's bonding strength and flexibility by dissolving various adhesive components effectively.
Used in Pharmaceuticals:
In the pharmaceutical industry, 2-Pyrrolidinone,1-[(2R)-oxiranylmethyl]-(9CI) serves as a solvent for the dissolution of active pharmaceutical ingredients, facilitating the manufacturing of various drug formulations.
It is crucial to handle 2-Pyrrolidinone,1-[(2R)-oxiranylmethyl]-(9CI) with care and adhere to proper safety protocols due to its potential hazards and risks associated with exposure. Despite these considerations, its unique properties and capabilities make it an indispensable component in a variety of applications across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 409335-13-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,9,3,3 and 5 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 409335-13:
(8*4)+(7*0)+(6*9)+(5*3)+(4*3)+(3*5)+(2*1)+(1*3)=133
133 % 10 = 3
So 409335-13-3 is a valid CAS Registry Number.
409335-13-3Relevant academic research and scientific papers
Synthesis of the enantiomers of 1-{2-Hydroxy-3-[4-(2-hydroxy-phenyl)- piperazin-1-yl ]-propyl}-pyrrolidin-2-one using soluble and polystyrene bound salenCo(III)OAc complexes as catalysts of hydrolytic kinetic resolution
Kulig,Nowicki,Malawska
, p. 179 - 186 (2008/02/11)
The asymmetric synthesis of 1-{2-hydroxy-3-[4-(2-hydroxy-phenyl)-piperazin- 1-yl]-propyl}-pyrrolidin-2-one 3 is described. Enantiomers of compound 3 were synthesized by hydrolytic kinetic resolution (HKR) of racemic 1-oxiranylmethyl-pyrrolidin-2-one rac-2
Stereocontrolled synthesis of the enantiomers of 1-[2-hydroxy-3-(4-phenyl-1-piperazinyl)-propyl]-pyrrolidin-2-one
Kulig, Katarzyna,Holzgrabe, Ulrike,Malawska, Barbara
, p. 2533 - 2536 (2007/10/03)
The asymmetric synthesis of 1-[2-hydroxy-3-(4-phenyl-1-piperazinyl)-propyl]-pyrrolidin-2-one 1 is described. Enantiomers of compound 1 were obtained using the Sharpless asymmetric dihydroxylation (AD) or hydrolytic kinetic resolution (HKR) methods. The enantiomers of compound 1, which were obtained by HKR had higher enantiomeric excesses than those which were synthesized by AD and epoxidation. The enantiomeric purity of the synthesized compounds was determinated by capillary electrophoresis.
