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(3S)-2,3-dihydro-3-(2-methylphenyl)-2-[(4-methylphenyl)sulfonyl]-1H-isoindol-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1365552-67-5

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1365552-67-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1365552-67-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,5,5,5 and 2 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1365552-67:
(9*1)+(8*3)+(7*6)+(6*5)+(5*5)+(4*5)+(3*2)+(2*6)+(1*7)=175
175 % 10 = 5
So 1365552-67-5 is a valid CAS Registry Number.

1365552-67-5Downstream Products

1365552-67-5Relevant academic research and scientific papers

Chiral-Directing-Group-Assisted Rhodium(III)-Catalyzed Asymmetric Addition of Inert Arene C?H Bond to Aldimines with Subsequent Intramolecular Cyclization

Cai, Xuhong,Chen, Wenkun,Nie, Ruifang,Wang, Jun

, p. 16611 - 16615 (2021/10/19)

By using a chiral directing group, an asymmetric rhodium(III)-catalyzed C?H bond addition to aldimines followed by intramolecular cyclization to form chiral isoindolinones has been achieved (up to 68 % yield, up to 93 % ee). A three-component variant that resembles Mannich reaction was also realized (41 % yield, 83 % ee). Product elaborations and preliminary mechanistic studies were described.

Rh(I)-catalyzed asymmetric synthesis of 3-substituted isoindolinones through co gas-free aminocarbonylation

Fujioka, Masahiko,Morimoto, Tsumoru,Tsumagari, Takayuki,Tanimoto, Hiroki,Nishiyama, Yasuhiro,Kakiuchi, Kiyomi

experimental part, p. 2911 - 2923 (2012/05/05)

A highly efficient and accessible synthesis of chiral 3-substituted isoindolinone frameworks is described. The synthesis involved the Rh(I)-catalyzed asymmetric arylation of boronic acids to 2-halobenzaldimines and the subsequent Rh(I)-catalyzed intramolecular aminocarbonylation of the resulting 2-halobenzylamines using an aldehyde as the carbonyl source. The method tolerates a variety of functional groups, yielding isoindolinone derivatives in moderate to high yields with high ee-values. In addition, two Rh(I)-catalyzed transformations could be efficiently accomplished in a one-pot sequence to give chiral isoindolinones by the simple addition of a ligand and an aldehyde after the Rh(I)-catalyzed asymmetric arylation.

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