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6,7-dimethoxy-1-(2-methoxyphenyl)isoquinoline is a complex organic compound belonging to the isoquinoline family, characterized by a tricyclic structure with two methoxy groups at positions 6 and 7, and a 2-methoxyphenyl substituent at position 1. 6,7-dimethoxy-1-(2-methoxyphenyl)isoquinoline is known for its potential applications in the pharmaceutical and chemical industries, particularly in the synthesis of various drugs and intermediates. Its molecular formula is C18H17NO3, and it exhibits a molecular weight of 293.33 g/mol. The compound's structure and properties make it a valuable research subject for chemists and biologists, as it may possess unique biological activities and potential therapeutic applications.

3161-11-3

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3161-11-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3161-11-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,6 and 1 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3161-11:
(6*3)+(5*1)+(4*6)+(3*1)+(2*1)+(1*1)=53
53 % 10 = 3
So 3161-11-3 is a valid CAS Registry Number.

3161-11-3Downstream Products

3161-11-3Relevant academic research and scientific papers

Strategies and synthetic methods directed toward the preparation of libraries of substituted isoquinolines

Awuah, Emelia,Capretta, Alfredo

supporting information; experimental part, p. 5627 - 5634 (2010/11/03)

Strategies for the production of substituted isoquinoline libraries were developed and explored. Routes involving microwave-assisted variants of the Bischler-Napieralski or Pictet-Spengler reaction allowed for cyclization of substituted β-arylethylamine derivatives. The dihydroisoquinolines and tetrahydroisoquinolines thus generated could then be oxidized to their corresponding isoquinoline analogues. An alternate strategy, however, involving the preparation and activation of isoquinolin-1(2H)-ones is demonstrated to be a more practical, rapid, and efficient route to C1- and C4-substituted isoquinoline libraries.

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