872358-02-6 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
(5R)-5-cyclohexyl-2-Pyrrolidinone is used as a building block in organic chemistry for the synthesis of pharmaceuticals and agrochemicals. Its unique structure allows it to be incorporated into complex molecules, contributing to the development of new drugs and pesticides.
Used in Polymer and Resin Production:
(5R)-5-cyclohexyl-2-Pyrrolidinone is used as a solvent in the production of polymers and resins. Its solubility properties make it suitable for use in the manufacturing process, aiding in the formation of desired polymer structures.
Used in Materials Science:
(5R)-5-cyclohexyl-2-Pyrrolidinone has potential applications in the field of materials science. Its ability to participate in various chemical reactions allows it to be used in the development of new materials with specific properties.
Used as a Chiral Auxiliary in Organic Synthesis:
(5R)-5-cyclohexyl-2-Pyrrolidinone is used as a chiral auxiliary in organic synthesis. Its stereochemistry can be exploited to control the selectivity of reactions, leading to the production of enantiomerically pure compounds, which are important in various applications, including pharmaceuticals and agrochemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 872358-02-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,2,3,5 and 8 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 872358-02:
(8*8)+(7*7)+(6*2)+(5*3)+(4*5)+(3*8)+(2*0)+(1*2)=186
186 % 10 = 6
So 872358-02-6 is a valid CAS Registry Number.
872358-02-6Relevant articles and documents
Synthesis of γ-, δ-, and ε-lactams by asymmetric transfer hydrogenation of N-(tert-butylsulfinyl)iminoesters
Guijarro, David,Pablo, Oscar,Yus, Miguel
, p. 3647 - 3654 (2013/05/22)
Highly enantiomerically enriched γ- and δ-lactams have been prepared by a simple and very efficient procedure that involves the asymmetric transfer hydrogenation of N-(tert-butylsulfinyl)iminoesters followed by desulfinylation of the nitrogen atom and spo
N-heterocyclic carbene and Bronsted acid cooperative catalysis: Asymmetric synthesis of trans -γ-Lactams
Zhao, Xiaodan,Dirocco, Daniel A.,Rovis, Tomislav
, p. 12466 - 12469 (2011/09/16)
An efficient enantioselective approach to form trans-γ-lactams in up to 99% yield, 93% ee, and >20/1 dr using unactivated imines has been developed. The cyclohexyl-substituted azolium and the weak base sodium o-chlorobenzoate are most suitable for this tr