102321-59-5 Usage
Description
N-[(2,3-dimethoxyphenyl)methyl]-3,4-dimethoxy-benzeneethanamine hydrochloride is a complex organic chemical compound characterized by a benzene ring with three methoxy groups and an amine group, which is in the form of a hydrochloride salt. This structure suggests its potential pharmaceutical applications, given the presence of the hydrochloride salt, although the specific medical uses would necessitate additional context or information regarding its pharmacological properties.
Uses
Given the lack of specific application details in the provided materials, the following uses are inferred based on the compound's characteristics as a pharmaceutical compound:
Used in Pharmaceutical Industry:
N-[(2,3-dimethoxyphenyl)methyl]-3,4-dimethoxy-benzeneethanamine hydrochloride is used as a pharmaceutical compound for its potential therapeutic effects, which may include the treatment of various medical conditions. The exact applications would be determined by its pharmacological profile and clinical trials.
Without further information on the specific applications or industries where this compound is utilized, it is not possible to provide more detailed uses. However, the presence of the hydrochloride salt and the compound's structure hint at its possible role in the development of new drugs or therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 102321-59-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,3,2 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 102321-59:
(8*1)+(7*0)+(6*2)+(5*3)+(4*2)+(3*1)+(2*5)+(1*9)=65
65 % 10 = 5
So 102321-59-5 is a valid CAS Registry Number.
102321-59-5Relevant articles and documents
Synthesis method of 13-methyl berberine alkaloid
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Paragraph 0044-0050; 0054-0057, (2022/03/17)
The invention belongs to the field of organic synthesis, and particularly relates to a synthesis method of 13-methyl berberine alkaloid. The method comprises the following steps: reaction a: taking arylethylamine and aryl formaldehyde as main starting raw materials, and reacting in the presence of other auxiliary materials to obtain secondary amine hydrochloride; and reaction b: taking secondary amine hydrochloride and pyruvic aldehyde as main raw materials, and reacting in the presence of other auxiliary materials to obtain the 13-methyl berberine alkaloid. According to the invention, aryl ethylamine and aryl formaldehyde are used as raw materials to synthesize secondary amine hydrochloride, and then the secondary amine hydrochloride and pyruvic aldehyde are subjected to Pickering-Schengger reaction/Friedel-Crafts hydroxyalkylation reaction/dehydration reaction/oxidation reaction in an anhydrous formic acid solution under the assistance of a dewatering agent and an oxidizing agent, so that the 13-methylberberine alkaloid is prepared at the yield of more than 80%, and the synthesis steps are simplified and easy to operate; and various expensive metal catalysts and excessive acid catalysis are not needed, the productivity is high, and the cost is low.
