189000-39-3 Usage
Uses
Used in Chemical Research and Synthesis:
2,2-Pyrrolidinedicarboxylic acid, 1-(4-chlorophenyl)-3-(2-naphthalenyl)-5-oxo-, diethyl ester is used as a chemical intermediate for the synthesis of other organic compounds. Its unique structure, which includes a chlorophenyl and naphthalenyl group, may contribute to the development of new chemical entities with potential applications in various fields.
Used in Pharmaceutical Development:
Although not widely documented, the presence of a chlorophenyl and naphthalenyl group in the structure of 2,2-Pyrrolidinedicarboxylic acid, 1-(4-chlorophenyl)-3-(2-naphthalenyl)-5-oxo-, diethyl ester suggests potential biological activity. This makes it a candidate for further research and development in the pharmaceutical industry, where it could be used as a building block for the creation of new drugs or as a starting material for the synthesis of bioactive molecules.
Used in Organic Chemistry:
2,2-Pyrrolidinedicarboxylic acid, 1-(4-chlorophenyl)-3-(2-naphthalenyl)-5-oxo-, diethyl ester is used as a research tool in organic chemistry, where it can be employed to study the reactivity and properties of its functional groups. This knowledge can be applied to the design and synthesis of new organic compounds with potential applications in various industries, such as materials science, agrochemistry, and pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 189000-39-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,9,0,0 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 189000-39:
(8*1)+(7*8)+(6*9)+(5*0)+(4*0)+(3*0)+(2*3)+(1*9)=133
133 % 10 = 3
So 189000-39-3 is a valid CAS Registry Number.
189000-39-3Relevant academic research and scientific papers
Chemoselective reduction of a lactam carbonyl group in the presence of a gem-dicarboxylate by sodium borohydride and iodine: A facile entry to N-aryl trisubstituted pyrroles
Haldar, Pranab,Ray, Jayanta K.
, p. 8229 - 8231 (2007/10/03)
Several N-aryl γ-lactam gem dicarboxylates were chemoselectively reduced to cyclic amine diesters by using sodium borohydride-iodine system. The reduction in all cases was completed within 2.5 h after refluxing in THF. The cyclic amine products were isolated after aqueous (acidic) workup in good yields. Hydrolytic decarboxylation followed by dehydrogenation produced N-aryl carboethoxy pyrroles.
Studies on γ-Lactams: Synthesis of some 3-Aryl-1, 3a,4,9b-tetrahydrobenzoindole-2,5-dione derivatives and its Implication in the Total Synthesis of Functionalized 17-Azasteroids
Kar, Gandhi K.,Ramesh, Dandala,Chatterjee, Basanta G.,Ray, Jayanta K.
, p. 568 - 583 (2007/10/03)
The γ-lactam diesters 3 and 10, prepared from anilinomalonates and 3-arylacryloyl chloride by intermolecular Michael addition followed by intramolecular amidification, were hydrolysed and selectively decarboxylated to the trans acids 4 and 11.Homologation by Arndt-Eistert's method followed by PPA cyclization produced the tri- and tetracyclic γ-lactam derivatives (8 and 15) simulating the B-C-D/A-B-C-D ring system of many azasteroids, in good overall yield.
