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1-(3-{(2Z)-3-methyl-2-[(oxoammonio)methylidene]-2,3-dihydro-1H-imidazol-1-yl}propyl)-3-oxo-1-azoniabicyclo[2.2.2]octane dibromide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

208182-95-0

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208182-95-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 208182-95-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,8,1,8 and 2 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 208182-95:
(8*2)+(7*0)+(6*8)+(5*1)+(4*8)+(3*2)+(2*9)+(1*5)=130
130 % 10 = 0
So 208182-95-0 is a valid CAS Registry Number.

208182-95-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name [(Z)-[1-methyl-3-[3-(3-oxo-1-azoniabicyclo[2.2.2]octan-1-yl)propyl]imidazol-2-ylidene]methyl]-oxoazanium,dibromide

1.2 Other means of identification

Product number -
Other names [(Z)-[1-methyl-3-[3-(3-oxo-1-azoniabicyclo[2.2.2]octan-1-yl)propyl]imidazol-2-ylidene]methyl]-oxoazanium dibromide

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:208182-95-0 SDS

208182-95-0Downstream Products

208182-95-0Relevant academic research and scientific papers

Quinuclidinium-imidazolium compounds: Synthesis, mode of interaction with acetylcholinesterase and effect upon Soman intoxicated mice

Simeon-Rudolf, Vera,Reiner, Elsa,Skrinjaric-Spoljar, Mira,Radic, Bozica,Lucic, Ana,Primozic, Ines,Tomic, Srdanka

, p. 289 - 295 (1998)

Four compounds were prepared: 3-oxo-1-methylquinuclidinium iodide (I), 2-hydroxyiminomethyl-1,3-dimethylimidazolium iodide (II) and two conjugates of I and II linked by -(CH2)3- (III) and -CH2-O-CH2- (IV). The aim was to evaluate separately the properties of I and II as opposed to III and IV, which contain both moieties in the same molecule. All four compounds were reversible inhibitors of acetylcholinesterase (AChE; EC 3.1.1.7). The enzyme/inhibitor dissociation constants for the catalytic site ranged from 0.073 mM (II) to 1.6 mM (I). The dissociation constant of I for the allosteric (substrate inhibition) site was 4.8 mM. Possible binding of the other compounds to the allosteric site could not be measured because II, III and IV reacted with the substrate acetylthiocholine (ATCh) and at high ATCh concentrations the non-enzymic reaction interfered with the enzymic hydrolysis of ATCh. The rate constants for the non-enzymic ATCh hydrolysis were between 23 and 37 l/mol per min. All four compounds protected AChE against phosphorylation by Soman and VX. The protective index (PI) of I (calculated from binding of I to both, catalytic and allosteric sites in AChE) agreed with the measured PI; this confirms that allosteric binding contributes to the decrease of phosphorylation rates. The PI values obtained with III and IV were higher than those predicted by the assumption of their binding to the AChE catalytic site only. The toxicity (i.p. LD50) of compounds I, II, III and IV for mice was 0.21, 0.68, 0.49 and 0.77 mmol/kg body wt. respectively. All four compounds protected mice against Soman when given (i.p.) together with atropine 1 min after Soman (s.c.). One-quarter of the LD50 dose fully protected mice (survival of all animals) against 2.52 (IV), 2.00 (I and III) and 1.58 (II) LD50 doses of Soman.

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