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Rac-N-methylanabasine is a synthetic organic compound with the chemical formula C10H14N2. It is a racemic mixture, meaning it consists of equal parts of both the R and S enantiomers. Rac-N-methylanabasine is structurally similar to anabasine, a naturally occurring alkaloid found in certain plants, and is known for its potential psychoactive effects. It is used in research settings to study the effects of anabasine and its derivatives on the nervous system. Due to its structural resemblance to nicotine, rac-N-methylanabasine has been investigated for its potential as a smoking cessation aid or as a component in the development of new medications targeting nicotine addiction. However, it is important to note that the compound's safety, efficacy, and legal status can vary by country, and it is not approved for medical use in many regions.

1966-44-5

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1966-44-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1966-44-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,6 and 6 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1966-44:
(6*1)+(5*9)+(4*6)+(3*6)+(2*4)+(1*4)=105
105 % 10 = 5
So 1966-44-5 is a valid CAS Registry Number.

1966-44-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name rac-N-methylanabasine

1.2 Other means of identification

Product number -
Other names (+/-)-N'-Methylanabasine

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:1966-44-5 SDS

1966-44-5Upstream product

1966-44-5Relevant academic research and scientific papers

From bipyridines to tobacco alkaloids and related compounds

Plaquevent, Jean-Christophe,Chichaoui, Ilhame

, p. 369 - 379 (2007/10/03)

Starting from structural considerations which led to the hypothesis that a chemical relationship could exist between two families of natural compounds (mainly pyridinic and pyrrolidinic alkaloids), experiments were carried out in order to establish a correlation route between the two studied classes. Of special interest was the central position of nicotine in these studies, and the main part of this work was devoted to the synthesis of nicotine starting from bipyridines. It was thus necessary to determine the conditions for selective reactions on one aromatic ring of bipyridines (N-methylation, N-oxidation and reduction of the heterocycle). Ring contraction procedure allowed us to obtain nicotine from the parent compound (3,3′-bipyridine). Complementary studies yielded various isomers of piperidinylpyridines (hexahydro derivatives of bipyridines) in a regiochemically controlled manner by means of original methods. Elsevier,.

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