3947-79-3 Usage
Chemical class
Quaternary ammonium compound
Structure
Contains multiple methoxy groups and a benzyl substituent
Derivative of
Isoquinoline
Common use
Pharmaceutical intermediate
Studied for
Potential antihypertensive and antiarrhythmic properties
Preclinical trials
Shown promising results
Investigated for
Potential use as a cholinesterase inhibitor
Role in treatment
Neurodegenerative diseases
Unique feature
Diverse potential applications
Research and development
Interesting target due to its unique chemical structure and diverse potential applications
Check Digit Verification of cas no
The CAS Registry Mumber 3947-79-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,4 and 7 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3947-79:
(6*3)+(5*9)+(4*4)+(3*7)+(2*7)+(1*9)=123
123 % 10 = 3
So 3947-79-3 is a valid CAS Registry Number.
3947-79-3Relevant academic research and scientific papers
SYTHESIS OF N-(ARYLETHYL)ARYLTHIOACETAMIDES BY THE WILLGERODT-KINDLER REACTION AND THEIR CONVERSION TO SUBSTITUTED 1-BENZYL-1,2,3,4-TETRAHYDROISOQUINOLINES
Nakova, E.P.,Tolkachev, O.N.,Evstigneeva, R.P.
, p. 550 - 555 (2007/10/02)
N-(Arylethyl)arylthioacetamides were synthesized by the reaction of substituted acetophenones with 2-arylethylamines.The reaction gives good yields when compounds with substituted hydroxyl groups are used. 2,4-Diarylthiazoles were isolated as side products from the Wilgerodt-Kindler reaction.The thioamides were converted into substituted 1-benzyl-1,2,3,4-tetrahydroisoquinolines by the Bischler-Napieralski cyclization, N-methylation, and reduction of the corresponding 3,4-dihydroisoquinoline methiodide derivatives.
