47235-20-1 Usage
Uses
Used in Pharmaceutical Industry:
3-(Benzyl(methyl)amino)-1-(3-methoxyphenyl)-2-methylpropan-1-one is used as a chemical intermediate for the synthesis of various drugs and pharmaceutical products. Its unique structure and functional groups contribute to the development of novel therapeutic agents with potential applications in treating specific medical conditions.
Used in Research and Development:
In the field of organic chemistry, 3-(Benzyl(methyl)amino)-1-(3-methoxyphenyl)-2-methylpropan-1-one serves as a research chemical, facilitating the study of organic reactions and the exploration of new pharmaceutical compounds. Its complex structure and potential reactivity make it a valuable tool for advancing scientific understanding and innovation in drug discovery.
Check Digit Verification of cas no
The CAS Registry Mumber 47235-20-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,7,2,3 and 5 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 47235-20:
(7*4)+(6*7)+(5*2)+(4*3)+(3*5)+(2*2)+(1*0)=111
111 % 10 = 1
So 47235-20-1 is a valid CAS Registry Number.
InChI:InChI=1S/C19H23NO2/c1-15(13-20(2)14-16-8-5-4-6-9-16)19(21)17-10-7-11-18(12-17)22-3/h4-12,15H,13-14H2,1-3H3
47235-20-1Relevant academic research and scientific papers
PROCESS FOR THE SYNTHESIS OF TAPENTADOL AND INTERMEDIATES THEREOF
-
Paragraph 0081; 0082; 0083, (2013/07/19)
The object of the present invention is a new process for the synthesis of tapentadol, both as free base and in hydrochloride form, which comprises the step of alkylation of the ketone (VII) to yield the compound (VIII), as reported in Diagram 1, with high
NEW PROCESS FOR THE SYNTHESIS OF TAPENTADOL AND INTERMEDIATES THEREOF
-
Page/Page column 4; 13-14, (2012/01/14)
The object of the present invention is a new process for the synthesis of tapentadol, both as free base and in hydrochloride form, which comprises the step of alkylation of the ketone (VII) to yield the compound (VIII), as reported in Diagram 1, with high
