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2-(3,4-dimethoxyphenethyl)-6,7-dimethoxyisoindolin-1-one is a complex organic compound with the molecular formula C20H21NO5. It is characterized by a central isoindolin-1-one ring, which is a type of cyclic structure with a carbonyl group attached to a nitrogen atom. The compound features a phenethyl side chain at the 2-position, which is substituted with two methoxy groups at the 3 and 4 positions. Additionally, the isoindolin-1-one ring has two methoxy groups at the 6 and 7 positions, enhancing its solubility and potentially affecting its chemical reactivity. This molecule is of interest in the field of organic chemistry, potentially for its pharmacological properties or as a building block in the synthesis of more complex molecules.

3344-74-9

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3344-74-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3344-74-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,4 and 4 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3344-74:
(6*3)+(5*3)+(4*4)+(3*4)+(2*7)+(1*4)=79
79 % 10 = 9
So 3344-74-9 is a valid CAS Registry Number.

3344-74-9Relevant academic research and scientific papers

A simple approach for the synthesis of azocine alkaloids: The total synthesis of megallanesine

Volvoikar, Prajesh S.,Tilve, Santosh G.

, p. 2567 - 2569 (2018)

A new three step synthetic route to construct azocine ring system using anion chemistry and intramolecular Friedel-Craft reaction of an ester is presented. This method allows synthesis of azocine ring analogues in excellent overall yields. The designed strategy was applied for the synthesis of naturally occurring magallanesine.

A practical and highly efficient synthesis of lennoxamine and related isoindolobenzazepines

Sahakitpichan, Poolsak,Ruchirawat, Somsak

, p. 4169 - 4172 (2007/10/03)

Lennoxamine and related isoindolobenzazepines were prepared in high yield by intramolecular condensation of aldehyde isoindolones under basic conditions followed by catalytic hydrogenation of the resulting dehydroisoindolobenzazepines.

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