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Anabaseine is a naturally occurring neurotoxin derived from hoplonemertine sea worms. It is known for its ability to compete with the natural neurotransmitter acetylcholine when binding to nicotinic receptor sites.

3471-05-4

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3471-05-4 Usage

Uses

Used in Pharmaceutical Industry:
Anabaseine is used as a therapeutic agent for the treatment of nicotine addiction and smoking cessation. Its ability to compete with acetylcholine at nicotinic receptor sites helps to reduce cravings and withdrawal symptoms associated with nicotine dependence.
Used in Neurological Research:
Anabaseine is used as a research tool in the study of nicotinic acetylcholine receptors and their role in various neurological disorders. Its interaction with these receptors provides valuable insights into the development of potential treatments for conditions such as Alzheimer's disease, Parkinson's disease, and schizophrenia.
Used in Toxicological Studies:
Anabaseine is used in toxicological research to understand the mechanisms of action and potential risks associated with neurotoxins. This knowledge can contribute to the development of antidotes and preventive measures against the harmful effects of similar toxins.

Check Digit Verification of cas no

The CAS Registry Mumber 3471-05-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,7 and 1 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3471-05:
(6*3)+(5*4)+(4*7)+(3*1)+(2*0)+(1*5)=74
74 % 10 = 4
So 3471-05-4 is a valid CAS Registry Number.

3471-05-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2,3,4,5-tetrahydropyridin-6-yl)pyridine

1.2 Other means of identification

Product number -
Other names anabaseine dihydrochloride

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:3471-05-4 SDS

3471-05-4Relevant academic research and scientific papers

Synthesis of cyclic imines via ethylenetetramethyldisilyl-protected ω-aminoimines. Application to the synthesis of alkaloids

De Kimpe, Norbert G.,Kepppens, Marian A.,Stevens, Christian V.

, p. 4693 - 4696 (1993)

Cyclic imines, including several alkaloids such as myosmine, anabaseine and apoferrorosamine, were synthesized by α-alkylation of imines with ethylenetetramethyldisilyl-protected ω-bromoamines, followed by ring closure.

Method for synthesis of 4-OH substituted anabaseine derivative

-

Page/Page column 3; 5; 6, (2017/03/08)

A method for synthesis of 4-OH substituted anabaseine derivative which is used as an α7 receptor agonist is revealed. A nucleophilic substitution reaction of δ-valerolactam with ethyl nicotinate is carried out to get an intermediate product. Th

The reaction of cyclic imines with the Ruppert-Prakash reagent. Facile approach to α-trifluoromethylated nornicotine, anabazine, and homoanabazine

Shevchenko, Nikolay E.,Vlasov, Katja,Nenajdenko, Valentine G.,R?schenthaler, Gerd-Volker

scheme or table, p. 69 - 74 (2011/02/27)

We have demonstrated that the Ruppert-Prakash reagent is able to react with a number of cyclic imines under acidic condition to afford the corresponding α-trifluoromethyl derivatives of nitrogen heterocycles. 5-7-Membered cyclic imines bearing various alkyl, aryl or heterocyclic group were successfully involved in this transformation. Novel trifluoromethylated analogues of nicotine, anabasine, and homoanabasine alkaloids were synthesized.

Organometallic Ring-Opening Reactions of N-Acyl and N-Alkoxycarbonyl Lactams. Synthesis of Cyclic Imines

Giovannini, Arianna,Savoia, Diego,Umani-Ronchi, Achille

, p. 228 - 234 (2007/10/02)

The reactions of hexyl- and phenylmagnesium bromides with N-acyl and N-alkoxycarbonyl lactams in tetrahydrofuran at -78 deg C have been performed to determine the factors affecting the regioselectivity.N-Pivaloyl γ- and δ-lactams undergo the ring-opening reactions with both Grignard reagents, whereas on the N-benzoyl γ-lactam a complete selectivity is achieved only with phenylmagnesium bromide.The N-Cbz γ- and δ-lactams preferentially react at the exocyclic carbonyl group, especially with hexylmagnesium bromide.The N-Boc five- to eight-membered lactams undergo the ring-opening reaction to give N-Boc-ω-amino ketones, although the efficiency slightly decreases by increasing the ring size.The deprotection of the N-Boc-ω-amino ketones with trifluoroacetic acid easily affords the corresponding five- to seven-membered cyclic imines.Pyridine alkaloids containing the cyclic imine moiety have been prepared by a modified route, exploiting the more easily available pyridyllithium reagents, instead of the corresponding Grignard reagents.

SYNTHESIS OF TOBACCO ALKALOIDS VIA TERTIARY AZIDES

Alberici, Gilles F.,Andrieux, Jean,Adam, Gerard,Plat, Michel M.

, p. 1937 - 1940 (2007/10/02)

A convenient new synthesis of different tobacco alkaloids, such as nicotine and anabasine is described, using as key step the SCHMIDT reaction applied to tertiary alcohols.

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