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166374-43-2

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166374-43-2 Usage

Uses

(±)-Epibatidine Dihydrochloride is an alkaloid and an α4β2 selective nicotinic agonist (1). It has binding affinities for α4β2 and α3β4 nicotinic receptors (2).

Check Digit Verification of cas no

The CAS Registry Mumber 166374-43-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,6,3,7 and 4 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 166374-43:
(8*1)+(7*6)+(6*6)+(5*3)+(4*7)+(3*4)+(2*4)+(1*3)=152
152 % 10 = 2
So 166374-43-2 is a valid CAS Registry Number.

166374-43-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (+)-Epibatidine dihydrochloride

1.2 Other means of identification

Product number -
Other names exo-(+)-1R,2R,4S-2-(6-Chloro-3-pyridinyl)-7-azabicyclo[2.2.1]heptane 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:166374-43-2 SDS

166374-43-2Downstream Products

166374-43-2Relevant articles and documents

The Synthesis of (+)- and (-)-Epibatidine

Fletcher, Stephen R.,Baker, Raymond,Chambers, Mark S.,Hobbs, Sarah C.,Mitchell, Paul J.

, p. 1216 - 1218 (2007/10/02)

The synthesis of the alkaloid epibatidine heptane> in enantiomeric form involving, as the critical step, reaction or 5-lithio-2-chloropyridine with N-tert-butoxycarbonyl-7-azabicycloheptan-2-one is des

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