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92118-22-4

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92118-22-4 Usage

Chemical Properties

Oil

Uses

Different sources of media describe the Uses of 92118-22-4 differently. You can refer to the following data:
1. A nicotine analogue
2. A novel Nicotine (N412420) analogue, a neuronal nicotinic receptor.

Check Digit Verification of cas no

The CAS Registry Mumber 92118-22-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,1,1 and 8 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 92118-22:
(7*9)+(6*2)+(5*1)+(4*1)+(3*8)+(2*2)+(1*2)=114
114 % 10 = 4
So 92118-22-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H14N2/c1-12-6-4-10(8-12)9-3-2-5-11-7-9/h2-3,5,7,10H,4,6,8H2,1H3

92118-22-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(1-methylpyrrolidin-3-yl)pyridine

1.2 Other means of identification

Product number -
Other names Isonicotine

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:92118-22-4 SDS

92118-22-4Downstream Products

92118-22-4Relevant articles and documents

Regioselective synthesis of 3-aryl substituted pyrrolidines via palladium catalyzed arylation: Pharmacological evaluation for central dopaminergic and serotonergic activity

Sonesson, Clas,Wikstroem, Hakan,Smith, Martin W.,Svensson, Kjell,Carlsson, Arvid,Waters, Nicholas

, p. 241 - 246 (2007/10/03)

A series of 3-arylpyrrolidines has been synthesised via palladium catalyzed arylation and evaluated for dopaminergic and serotonergic activity in vitro and in vivo. Compounds substituted by electron withdrawing groups on the meta position of the aromatic ring, were found to be preferential dopamine autoreceptor antagonists.

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