65700-38-1 Usage
Chemical class
Alkaloids
It belongs to a group of naturally occurring organic compounds that contain mostly basic nitrogen atoms.
Derivative of
Tetrahydroisoquinoline
It is a modified version of the parent compound, tetrahydroisoquinoline, with additional functional groups.
1-(3,4-dimethoxybenzyl) group
A benzyl group with two methoxy groups attached to the 3rd and 4th carbon atoms.
6,7-dimethoxy-2-propyl group
A propyl group attached to the 2nd carbon atom, with two methoxy groups attached to the 6th and 7th carbon atoms.
Potential pharmaceutical and medicinal properties
Due to its structure and functional groups, it may have various biological activities.
Anti-inflammatory
It may help reduce inflammation in the body.
Analgesic
It may have the ability to relieve pain.
Neuroprotective
It may protect neurons and support brain health.
Pharmaceutical research
It can be studied for its potential therapeutic effects and uses in medicine.
Chemical synthesis
It can be used as a building block or intermediate in the synthesis of other complex molecules.
Specific uses and effects
These may vary depending on the specific applications in pharmaceutical research or chemical synthesis.
Further research needed
More studies are required to fully understand the compound's properties, potential applications, and mechanisms of action.
Check Digit Verification of cas no
The CAS Registry Mumber 65700-38-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,7,0 and 0 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 65700-38:
(7*6)+(6*5)+(5*7)+(4*0)+(3*0)+(2*3)+(1*8)=121
121 % 10 = 1
So 65700-38-1 is a valid CAS Registry Number.
65700-38-1Relevant 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.
