56365-73-2 Usage
Uses
Used in Pharmaceutical Industry:
Methyl 2-phenyl-2H-isoindole-1-carboxylate is used as an intermediate for the synthesis of various pharmaceuticals, contributing to the development of new drugs and materials. Its versatile reactivity and functional groups make it a valuable component in medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, methyl 2-phenyl-2H-isoindole-1-carboxylate is used as an intermediate in the production of agrochemical products, playing a role in the development of new compounds for agricultural applications.
Used in Research and Development:
Methyl 2-phenyl-2H-isoindole-1-carboxylate is also commonly employed in research and development processes, where it aids in the creation and study of novel drugs and materials, further expanding its utility in scientific advancement.
Check Digit Verification of cas no
The CAS Registry Mumber 56365-73-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,3,6 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 56365-73:
(7*5)+(6*6)+(5*3)+(4*6)+(3*5)+(2*7)+(1*3)=142
142 % 10 = 2
So 56365-73-2 is a valid CAS Registry Number.
56365-73-2Relevant academic research and scientific papers
Selective synthesis of either isoindole- or isoindoline-1-carboxylic acid esters by Pd(0)-catalyzed enolate arylation
Sole, Daniel,Serrano, Olga
experimental part, p. 6267 - 6270 (2010/12/19)
Figure presented. Two efficient palladium-catalyzed intramolecular α-arylation reactions of α-amino acid esters have been developed that allow either 1-isoindolecarboxylic acid esters or the corresponding isoindolines to be selectively synthesized simply by a slight change of reaction conditions.
Palladium-catalysed synthesis of 1-isoindolecarboxylic acid esters and sequential Diels-Alder reactions: Access to bridged- and fused-ring heterocycles
Sole, Daniel,Serrano, Olga
supporting information; experimental part, p. 3382 - 3384 (2010/01/06)
The Pd-catalysed intramolecular α-arylation of α-amino acid esters provides a useful methodology for the synthesis of substituted isoindole derivatives, which have been used in Diels-Alder reactions to access diverse skeletal frameworks.
