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10,11-dimethoxy-5,6,7,8-tetrahydrodibenzo[c,e]azocine is a complex organic compound belonging to the class of azocines, which are a type of azepine. This specific compound is characterized by its unique molecular structure, featuring a dibenzo[c,e]azocine core with a tetrahydro ring system. The presence of two methoxy groups at the 10 and 11 positions further distinguishes 10,11-dimethoxy-5,6,7,8-tetrahydrodibenzo[c,e]azocine. It is known for its potential applications in the pharmaceutical industry, particularly in the development of drugs targeting the central nervous system. Due to its complex structure, the synthesis of 10,11-dimethoxy-5,6,7,8-tetrahydrodibenzo[c,e]azocine requires advanced chemical techniques and is of interest to researchers in the field of medicinal chemistry.

64906-08-7

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64906-08-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64906-08-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,9,0 and 6 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 64906-08:
(7*6)+(6*4)+(5*9)+(4*0)+(3*6)+(2*0)+(1*8)=137
137 % 10 = 7
So 64906-08-7 is a valid CAS Registry Number.

64906-08-7Downstream Products

64906-08-7Relevant academic research and scientific papers

Generation of a small library of highly electron-rich 2-(hetero)aryl- substituted phenethylamines by the Suzuki-Miyaura reaction: A short synthesis of an apogalanthamine analogue

Appukkuttan, Prasad,Orts, Amparo Baiget,Chandran, R. Prakash,Goeman, Jan. L.,Van Der Eycken, Johan,Dehaen, Wim,Van Der Eycken, Erik

, p. 3277 - 3285 (2004)

The Suzuki-Miyaura reaction is presented as a versatile procedure for the synthesis of a small library of highly electronrich 2-[4,5-dimethoxy-2-(hetero) arylphenyl]ethylamines. Microwave-irradiation accelerates the reaction tremendously and furnishes superior yields. The difficult oxidative addition of the catalyst to a highly electron-rich and ortho-substituted system could be performed easily, and the proto-deboronation during cross-coupling reactions involving the highly electron-withdrawing (2-formylphenyl)boronic acid could be minimized. Enhanced yields and complete compatibility with aqueous conditions were found. This strategy was developed en route towards the synthesis of an apogalanthamine analogue. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004.

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