69-27-2 Usage
Description
Chlorisondamine diiodide is a chemical compound that acts as a biochemical probe in the study of nicotinic receptors. It is also used as an intracranial injection for the localization and analysis of small drug molecules in rat brain tissue.
Uses
Used in Biochemical Research:
Chlorisondamine diiodide is used as a biochemical probe for studying nicotinic receptors, which are important in the nervous system and have potential therapeutic applications.
Used in Neuroscience Research:
Chlorisondamine diiodide is used as an intracranial injection in rat brain tissue to study the localization and analysis of small drug molecules. This helps researchers understand the distribution and effects of these molecules in the brain, which can be useful for developing new treatments for neurological disorders.
Originator
Ecolid Chloride,Ciba,US,1956
Manufacturing Process
50 parts by weight of 3,4,5,6-tetrachlorophthalic anhydride is added with
stirring and cooling to 30 parts by volume of 2-dimethylaminoethyl amine.
The mixture is heated at 170°C for 4 minutes and the oily residue then
dissolved in 200 parts by volume of hot ethanol. On cooling, N-(2'-
dimethylaminoethyl)-3,4,5,6-tetrachlorophthalimide separates. It crystallizes
from ethanol and melts at 184°-186°C.
6 parts by weight of N-(2'-dimethylaminoethyl)-3,4,5,6-tetrachlorophthalimide
is extracted continuously with 300 parts by volume of dry ether in which have
been dissolved 3.1 parts by weight of lithium aluminum hydride. After 48
hours the excess lithium aluminum hydride is destroyed by cautious addition
of 9 parts by volume of ethyl acetate while stirring. There is then added in
succession with stirring 3 parts by volume of water, 6 parts by volume of 15%
aqueous sodium hydroxide and 9 parts by volume of water. The granular
precipitate of lithium and aluminum salts are filtered and washed with ether.
The ether is distilled off, yielding the crude, oily 4,5,6,7-tetrachloro-2-(2'-
dimethylaminoethyl)-isoindoline. The above base is dissolved in 25 parts by
volume of 90% ethanol and refluxed 2 hours with 6 parts by volume of methyl
iodide. 4,5,6,7-tetrachloro-2-(2'-dimethylaminoethyl)-isoindoline dimethiodide
separates during the reaction. It is collected by filtration and recrystallizedfrom a mixture of ethanol and water; MP 244°-246°C.
4,5,6,7-tetrachloro-2-(2'-dimethylaminoethyl)-isoindoline dimethochloride is
prepared by shaking an aqueous solution of the dimethiodide with an excess
of freshly prepared silver chloride and evaporating to dryness the aqueous
solution after removal of the silver salts. 4,5,6,7-tetrachloro-2-(2'-
dimethylaminoethyl)-isoindoline dimethochloride is recrystallized from ethanolethylacetate; MP 276°-280°C.
Therapeutic Function
Antihypertensive
Biological Activity
An exceptionally long lasting nicotinic antagonist (IC 50 ~ 1.6 mM); blockade of central nicotinic responses induced by chlorisondamine can persist for several weeks.
Check Digit Verification of cas no
The CAS Registry Mumber 69-27-2 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 6 and 9 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 69-27:
(4*6)+(3*9)+(2*2)+(1*7)=62
62 % 10 = 2
So 69-27-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H20Cl4N2.2HI/c1-19(2,3)5-6-20(4)7-9-10(8-20)12(16)14(18)13(17)11(9)15;;/h5-8H2,1-4H3;2*1H/q+2;;/p-2