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Nor-(-)-scopolamine, also known as scopolamine, is a naturally occurring tropane alkaloid found in plants such as Atropa belladonna, Datura stramonium, and Datura metel. It acts as a potent muscarinic antagonist, blocking the action of acetylcholine at muscarinic receptors in the parasympathetic nervous system. This results in various effects, including sedation, amnesia, and hallucinations. Scopolamine has been used medicinally for its anticholinergic properties, particularly in the treatment of motion sickness and as a pre-anesthetic medication. However, it is also known for its potential misuse as a "date rape" drug due to its ability to induce memory loss and disorientation. The chemical structure of nor-(-)-scopolamine consists of a tropane ring with a methylated nitrogen atom and a hydroxyl group, making it a significant compound in both medical and forensic contexts.

3292-20-4

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3292-20-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3292-20-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,9 and 2 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3292-20:
(6*3)+(5*2)+(4*9)+(3*2)+(2*2)+(1*0)=74
74 % 10 = 4
So 3292-20-4 is a valid CAS Registry Number.

3292-20-4Upstream product

3292-20-4Downstream Products

3292-20-4Relevant academic research and scientific papers

ELECTRON-TRANSFER ACTIVATION. SALT EFFECTS ON THE PHOTOOXADIDATION OF TERTIARY AMINES : A USEFUL N-DEMETHYLATION METHOD

Santamaria, J.,Ouchabane, R.,Rigaudy, J.

, p. 3977 - 3980 (1989)

Photooxidation of tertiary methylamines sensitized by electron acceptors like 9,10-dicyanoanthracene is shown to proceed by two distinct ways depending on the presence of added salts.In the absence of added salt both nor and N-formyl compounds were obtained while with added salt the nor-derivative is obtained highly efficiently.

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