110568-65-5 Usage
Uses
Used in Pharmaceutical Industry:
5,6-DIMETHYL-2,3-DIHYDRO-ISOINDOL-1-ONE is used as a key building block in the synthesis of various pharmaceutical products. Its versatile reactivity and structural properties allow for the development of new and innovative medications.
Used in Organic Synthesis:
5,6-DIMETHYL-2,3-DIHYDRO-ISOINDOL-1-ONE is utilized in organic synthesis processes, where it serves as an intermediate or a precursor for the production of other organic compounds. Its unique structure and reactivity make it a valuable component in the synthesis of a wide range of organic molecules.
Used in Agrochemical Industry:
5,6-DIMETHYL-2,3-DIHYDRO-ISOINDOL-1-ONE is also used in the agrochemical industry, where it is employed in the synthesis of various agrochemicals. Its properties make it suitable for the development of new and effective products for agricultural applications.
Used in Research and Development:
Due to its potential biological activities and pharmacological properties, 5,6-DIMETHYL-2,3-DIHYDRO-ISOINDOL-1-ONE is used in research and development for the discovery of new therapeutic agents and the study of its biological effects.
Check Digit Verification of cas no
The CAS Registry Mumber 110568-65-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,5,6 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 110568-65:
(8*1)+(7*1)+(6*0)+(5*5)+(4*6)+(3*8)+(2*6)+(1*5)=105
105 % 10 = 5
So 110568-65-5 is a valid CAS Registry Number.
110568-65-5Relevant academic research and scientific papers
Zhang, Chunhui,Ding, Yongzheng,Gao, Yuzhen,Li, Shangda,Li, Gang
, p. 2595 - 2598 (2018)
A protocol for palladium-catalyzed C-H carbonylation of readily available free primary benzylamines using NH2 as the chelating group under an atmospheric pressure of CO has been achieved, providing a general, atom- and step-economic approach to
Studies on the Chemistry of Isoindoles and Isoindolenines, XXVIII. - 3-Alkoxy-1H-isoindoles, Syntheses and Properties
Hennige, Hans,Kreher, Richard P.,Konrad, Michael,Jelitto, Frank
, p. 243 - 252 (2007/10/02)
3-Alkoxy-1H-isoindoles 1 bearing substituents at the carboxylic moiety have been synthesized from substituted 2,3-dihydro-1H-isoindol-1-ones 4 by regiospecific O-alkylation to 5 with trialkyloxonium tetrafluoroborates or methyl trifluoroborates or methyl trifluoromethanesulfonate and subsequent NH deprotonation.According to the spectroscopic properties the semicyclic alkyl imidates 1 exist exclusively in the benzoid 1H structure; the tautomeric o-quinonoid 2H structure 2 cannot be detected by spectroscopic means.
