59084-79-6 Usage
Uses
Used in Organic Synthesis:
6,7-DIMETHOXY-2,3-DIHYDRO-ISOINDOL-1-ONE is used as a key intermediate in the synthesis of various organic compounds. Its unique structure and reactivity make it a valuable building block for creating new molecules with specific functional groups and properties.
Used in Medicinal Chemistry:
In the pharmaceutical industry, 6,7-DIMETHOXY-2,3-DIHDRO-ISOINDOL-1-ONE is used as a starting material for the development of new drugs. Its potential biological activities and unique structure make it a promising candidate for medicinal chemistry research.
Used in Pharmaceutical Research:
6,7-DIMETHOXY-2,3-DIHYDRO-ISOINDOL-1-ONE is used as a subject of pharmaceutical research due to its potential biological activities. Its unique structure and reactivity may contribute to the discovery of new therapeutic agents.
Used in the Synthesis of Other Compounds:
6,7-DIMETHOXY-2,3-DIHYDRO-ISOINDOL-1-ONE is used as a building block for the synthesis of other compounds with specific functional groups and properties. Its unique structure allows for the creation of new molecules with potential applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 59084-79-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,0,8 and 4 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 59084-79:
(7*5)+(6*9)+(5*0)+(4*8)+(3*4)+(2*7)+(1*9)=156
156 % 10 = 6
So 59084-79-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H11NO3/c1-13-7-4-3-6-5-11-10(12)8(6)9(7)14-2/h3-4H,5H2,1-2H3,(H,11,12)
59084-79-6Relevant academic research and scientific papers
Application of the ortho-Lithiation-Cyclization Strategy to N-Benzyl- and N-Phenethylamine Derivatives
Lete, Esther,Collado, M. Isabel,Sotomayor, Nuria,Vicente, Teresa,Villa, Maria-Jesus
, p. 1751 - 1758 (2007/10/03)
The ortho-lithiation-cyclization of iodinated N,N-diacylphenethylamines provides a convenient method for the preparation of 2-(2-acetoamidoethyl)acetophenones and 2-(2-benzamidoethyl)benzophenones, which could be easily transformed into dihydroisoquinolines.By contrast, the N-ethylamino, N-acetylamino, and N-trimethylsilylamino moieties studied as ortho-directing groups provide poor assistance to the metalation of N-benzyl- and N-phenyethylamines and the corresponding isoindolone or isoquinolone derivatives are obtained in low yields.
