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Scopoline, also known as scopolamine, is a naturally occurring chemical compound belonging to the tropane alkaloid family. It is found in plants such as henbane, jimsonweed, and belladonna. Scopoline exhibits potent anticholinergic effects by blocking the action of the neurotransmitter acetylcholine in the central and peripheral nervous systems. This property makes it a valuable compound in various medical applications.

487-27-4

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487-27-4 Usage

Uses

Used in Pharmaceutical Industry:
Scopoline is used as an antiemetic and anti-motion sickness agent for its ability to alleviate nausea, vomiting, and motion sickness. It is particularly effective in treating these symptoms due to its potent anticholinergic effects.
Used in Surgical Procedures:
Scopoline is used as a sedative and anesthetic adjunct in patients undergoing surgery or medical procedures. Its calming and relaxing effects help to reduce anxiety and ensure a smoother surgical experience.
However, it is important to note that scopoline has the potential to cause hallucinations, amnesia, and delirium when used inappropriately at higher doses. Due to these risks and its potential for abuse, scopoline is classified as a controlled substance in many countries. This highlights the need for careful regulation and responsible use of scopoline in medical settings.

Check Digit Verification of cas no

The CAS Registry Mumber 487-27-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,8 and 7 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 487-27:
(5*4)+(4*8)+(3*7)+(2*2)+(1*7)=84
84 % 10 = 4
So 487-27-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H13NO2/c1-9-5-2-4-3-6(9)8(11-4)7(5)10/h4-8,10H,2-3H2,1H3/t4-,5-,6+,7+,8-/m0/s1

487-27-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Scopoline

1.2 Other means of identification

Product number -
Other names (+-)-3endo,7endo-Epoxy-tropan-6exo-ol,(+-)-Oscin

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:487-27-4 SDS

487-27-4Relevant academic research and scientific papers

Enzymatic Resolution of Tropinone Derivatives

Cramer, Nicolai,Laschat, Sabine,Baro, Angelika

, p. 2178 - 2181 (2007/10/03)

The lipase-mediated kinetic resolution of racemic scopoline [(±)-4] and 6-hydroxytropinone [(±)-7] is reported. Whereas (±)-4 is difficult to resolve due to steric hindrance of the hydroxy function, the resolution of (±)-7 with vinyl acetate as acyl donor gave alcohol (+)-7 and the corresponding acetate (-)-9 with high enantiomeric excess. In case of the optimal result of 99% ee for (+)-7 and 80% ee for (-)-9, an E-value of 35 was calculated. The preparative lipase-catalyzed resolution of (±)-7 resulted in almost enantiopure alcohol (+)-7 with >99% ee after one recrystallization.

An Efficient Route to the Tropane Alkaloids

Mann, John,Barbosa, Luiz-Claudio de Almeida

, p. 787 - 790 (2007/10/02)

We describe the use of diethylzinc in conjunction with polybromo ketones for the production of oxyallyls, and the interception of these intermediates by furans and methyl pyrrole-N-carboxylate.This methodology allows the production of gramme quantities of tropane alkaloids, and 2-substituted 8-oxabicyclooct-6-en-3-ones that have been either difficult or impossible to prepare.

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