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Quinolinium, 2-[(dithiocarboxy)methyl]-1,6-dimethyl-, hydroxide, inner salt is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

67943-66-2

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67943-66-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67943-66-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,9,4 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 67943-66:
(7*6)+(6*7)+(5*9)+(4*4)+(3*3)+(2*6)+(1*6)=172
172 % 10 = 2
So 67943-66-2 is a valid CAS Registry Number.
InChI:InChI=1/C13H15NS2/c1-9-3-6-12-10(7-9)4-5-11(14(12)2)8-13(15)16/h3-7,11H,8H2,1-2H3,(H,15,16)

67943-66-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Quinolinium, 2-[(dithiocarboxy)methyl]-1,6-dimethyl-, hydroxide, inner salt

1.2 Other means of identification

Product number -
Other names 2-(1,6-dimethylquinolin-2-yl)ethanedithioate

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:67943-66-2 SDS

67943-66-2Relevant academic research and scientific papers

Antileukemic activity of 2-bis(2-methylthio)vinyl-1-methylquinolinium iodides

Foye,Kauffman

, p. 477 - 480 (2007/10/02)

Reaction of 1-methylquinolinium-2-dithioacetic acid zwitterions with excess methyl iodide in dimethylformamide gave the corresponding bis(2-methylthio)vinyl derivatives. These compounds were more soluble in both aqueous and organic media than the dithioacetic acid zwitterions but showed comparable antileukemic activity in mice. Reaction with morpholine converted a bis(2-methylthio)vinyl derivative almost quantitatively to the 2-mono(methylthio)-2-morpholino derivative. Leukemia cell culture studies of the 6-methyl derivative showed no effect on cell cycle processes.

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