20412-86-6 Usage
Uses
Used in Pharmaceutical Applications:
1-(3,4-dimethoxy-benzyl)-2-ethyl-6,7-dimethoxy-1,2,3,4-tetrahydro-isoquinoline is used as a potential ligand in the pharmaceutical industry for its ability to interact with different biological targets such as receptors or enzymes. Its specific application reason is attributed to its unique structural features that may allow it to modulate or bind to these targets, thus influencing their activity.
Further research is necessary to fully understand the pharmacological properties and explore the potential therapeutic uses of 1-(3,4-dimethoxy-benzyl)-2-ethyl-6,7-dimethoxy-1,2,3,4-tetrahydro-isoquinoline. As it stands, 1-(3,4-dimethoxy-benzyl)-2-ethyl-6,7-dimethoxy-1,2,3,4-tetrahydro-isoquinoline is a promising candidate for drug development, particularly in the areas where its interaction with biological targets could lead to novel treatments or therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 20412-86-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,4,1 and 2 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 20412-86:
(7*2)+(6*0)+(5*4)+(4*1)+(3*2)+(2*8)+(1*6)=66
66 % 10 = 6
So 20412-86-6 is a valid CAS Registry Number.
20412-86-6Relevant academic research and scientific papers
Simple and selective one-pot replacement of the N-methyl group of tertiary amines by quaternization and demethylation with sodium sulfide or potassium thioacetate: An application to the synthesis of pergolide
Anastasia,Cighetti,Allevi
, p. 2398 - 2403 (2007/10/03)
The paper describes a mild, selective, and rapid replacement of an N-methyl group of tertiary amines with other alkyl groups via a simple one-pot procedure. This transformation is easily achieved by preparation of the appropriate quaternary ammonium salt in sulfolane and in situ treatment with sodium sulfide or potassium thioacetate. The protocol is successfully applied to the transformation of dihydrolysergol, dextromethorphan and laudanosine (as models of ergot and opium N-methyl alkaloids) into various N-alkyl congeners.
