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1-Benzyl-2-formyl-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline is a complex organic compound belonging to the isoquinoline family. It features a tetrahydroisoquinoline core, which is a reduced form of isoquinoline, with a benzyl group attached to the nitrogen atom at position 1. The molecule also contains a formyl group (aldehyde) at position 2 and two methoxy groups at positions 6 and 7, which are electron-donating groups that can influence the compound's reactivity and stability. This chemical structure may be of interest in medicinal chemistry and drug design due to its potential biological activities and interactions with various receptors.

3972-79-0

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3972-79-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3972-79-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,7 and 2 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3972-79:
(6*3)+(5*9)+(4*7)+(3*2)+(2*7)+(1*9)=120
120 % 10 = 0
So 3972-79-0 is a valid CAS Registry Number.

3972-79-0Downstream Products

3972-79-0Relevant academic research and scientific papers

Synthesis of benzyl substituted tetrahydropyridines and 1,2,3,4- tetrahydroisoquinolines via acid catalyzed cyclization of γ,δ-unsaturated N-formyl-N-styryl amines

Meuzelaar, Gerrit J.,Maatz.ast, Leendert,Sheldon, Roger A.

, p. 4481 - 4488 (1999)

Acid-catalyzed cyclization of N-(3-methylbut-3-enyl)-N-styrylformamides 1-3 in the presence of 9-BBN triflate gave access to 2-benzyl-1-formyl-4- methyl-1,2,5,6-tetrahydropyridines 4a-6a and minor amounts of the isomeric 1,2,3,6-tetrahydropyridines 4b-6b.

Reductive formylation of isoquinoline derivatives with formamide and synthesis of 2-formyltetrahydroisoquinolines

Venkov, Atanas P.,Ivanov, Ilian I.

, p. 1433 - 1438 (2007/10/03)

Reductive formylation of isoquinoline derivatives as 3,4- dihydroisoquinolines 1, enamines and enamides of tetrahydroisoquinoline 2 and the reaction of 2-(2-acylphenyl)ethylamides 3 with formamide afforded the corresponding N-formyltetrahydroisoquinolines 4 and N- acyltetrahydroisoquinolines 5.

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