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2,3-dimethoxy-6-[(6-methyl-5,6,7,8-tetrahydro[1,3]dioxolo[4,5-g]isoquinolin-5-yl)methyl]benzaldehyde is a complex benzaldehyde derivative characterized by the presence of two methoxy groups and a tetrahydro[1,3]dioxolo[4,5-g]isoquinolin-5-yl functional group. This unique structure and properties make it a promising candidate for medicinal and pharmaceutical research.

62475-57-4

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62475-57-4 Usage

Uses

Used in Medicinal and Pharmaceutical Research:
2,3-dimethoxy-6-[(6-methyl-5,6,7,8-tetrahydro[1,3]dioxolo[4,5-g]isoquinolin-5-yl)methyl]benzaldehyde is used as a building block in the synthesis of other chemical compounds for medicinal and pharmaceutical research. Its unique structure and properties may exhibit biological activity, leading to the development of new drugs or treatments for various medical conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 62475-57-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,4,7 and 5 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 62475-57:
(7*6)+(6*2)+(5*4)+(4*7)+(3*5)+(2*5)+(1*7)=134
134 % 10 = 4
So 62475-57-4 is a valid CAS Registry Number.

62475-57-4Downstream Products

62475-57-4Relevant academic research and scientific papers

Chemical Transformation of Protoberberines. IV. A Novel, Simple Synthesis of (+/-)-Canadaline and a Retroprotoberberine from Tetrahydroberberine

Hanaoka, Miyoji,Nagami, Kazuyoshi,Inoue, Mitsuru,Yasuda, Shingo

, p. 2685 - 2690 (2007/10/02)

Heating of tetrahydroberberine (1) in ethyl chloroformate preferentially afforded the C8-N bond cleavage (4) with small amounts of the C6-N and C14-N bond cleavage products (5 and 6, respectively).The urethane (4) was effe

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