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(3aR,4,R7S,7aS)-2-(benzyloxy)-3a,4,7,7a-tetrahydro-1H-4,7-epoxyisoindole-1,3(2H)-dione is a complex organic compound with a unique molecular structure. It is characterized by its tetrahydro-1H-4,7-epoxyisoindole-1,3(2H)-dione core, which features a 4,7-epoxy bridge and a 1,3-dione functional group. compound The also has a benzyloxy substituent at the 2-position, which is attached to the molecule through an oxygen atom. The stereochemistry of the compound is defined by the (3aR,4R,7S,7aS) configuration, indicating the specific arrangement of atoms in the molecule. (3aR,4R,7S,7aS)-2-(benzyloxy)-3a,4,7,7a-tetrahydro-1H-4,7-epoxyisoindole-1,3(2H)-dione is of interest in the field of organic chemistry and may have potential applications in the synthesis of pharmaceuticals or other specialty chemicals.

32463-64-2

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32463-64-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 32463-64-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,4,6 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 32463-64:
(7*3)+(6*2)+(5*4)+(4*6)+(3*3)+(2*6)+(1*4)=102
102 % 10 = 2
So 32463-64-2 is a valid CAS Registry Number.

32463-64-2Relevant academic research and scientific papers

Three-Component Synthesis of Quinolines Based on Radical Cascade Visible-Light Photoredox Catalysis

Choi, Jun-Ho,Park, Cheol-Min

, p. 3553 - 3562 (2018)

Synthesis of highly substituted quinolines has been developed based on three-component radical cascade based on visible-light photoredox catalysis. This tandem coupling reaction has been coordinated to proceed with high chemoselectivity based on the differential electronic properties of coupling partners. Subjection of electron-rich β-aminoacrylates with electron-deficient halides and alkenes to the optimized conditions leads to the formation of quinolines in good yields after in situ oxidation of tetrahydroquinolines. Detailed mechanistic studies which reveal an unexpected reaction pathway is described. (Figure presented.).

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