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2-p-tolyl-1,4-dihydro-2H-isoquinolin-3-one is a chemical compound belonging to the isoquinolinone class, characterized by a fused ring structure consisting of an isoquinoline and a pyridine ring. This specific compound features a 2-p-tolyl group, which is a para-tolyl (4-methylphenyl) substituent attached to the isoquinoline core. The compound is a 1,4-dihydro derivative, indicating that it has two hydrogen atoms added across the 1,4 positions of the isoquinoline ring, which reduces the aromaticity and introduces a double bond between these positions. The 3-one functional group signifies the presence of a carbonyl group at the 3-position, which can participate in various chemical reactions and interactions. 2-p-tolyl-1,4-dihydro-2H-isoquinolin-3-one may have potential applications in medicinal chemistry, particularly in the development of drugs targeting specific receptors or enzymes, due to its unique structure and functional groups.

6772-69-6

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6772-69-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6772-69-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,7 and 2 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6772-69:
(6*6)+(5*7)+(4*7)+(3*2)+(2*6)+(1*9)=126
126 % 10 = 6
So 6772-69-6 is a valid CAS Registry Number.

6772-69-6Downstream Products

6772-69-6Relevant academic research and scientific papers

A new and facile approach to 1,2-dihydroisoquinolin-3(4: H)-imines by the Cu(i)-catalyzed reaction of 2-ethynylbenzyl methanesulfonates, sulfonyl azides and amines

Huang, Ying,Yi, Weiyin,Sun, Qihui,Zhang, Lirong,Yi, Fengping

, p. 74 - 79 (2018/01/17)

A new, step-economical and operationally simple access to unsubstituted 1,2-dihydroisoquinolin-3(4H)-imines by Cu-catalyzed MCRs under mild conditions is described. In addition, selective hydrolysis of imines to the corresponding 1,2-dihydroisoquinolin-3(4H)-ones under refluxed conc. HCl has also been investigated.

Synthetic approaches to 2-substituted 1-oxo- and 3-oxotetrahydroisoquinolines

Cheng,Tsai,Lin

, p. 73 - 77 (2007/10/02)

2-Substituted homophthalimides 2a-c were reduced regioselectively with sodium borohydride to carbinol-lactam intermediates 3a-c, which were dehydrated, followed by hydrogenation, to give 1-oxotetrahydroisoquinolines or 3,4-dihydroisoquinolin-1(2H)ones 5a-c. The isomeric 3-oxo-tetrahydroisoquinolines or 1,4-dihydroisoquinolin-3(2H)-ones 8a-i were obtained in satisfactory yields via heating 3-isochromanone (6) with the corresponding amines 7a-i in the presence of aluminum chloride.

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