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69282-16-2

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69282-16-2 Usage

Chemical Structure

A complex chemical compound with a piperidine group, a tetradecahydroanthracen-9-yl group, and a 1,2-dihydropyridine group connected in sequence.

Potential Applications

Pharmaceutical research, specifically in the development of new medications for cardiovascular disease and neurological disorders.

Unique Properties

The compound's structure and properties make it an interesting target for further study and potential drug development.

Research and Testing

Extensive testing and research would be needed to fully understand its potential uses and effects due to its complex nature.

Chemical Reactivity

The compound may exhibit reactivity with various reagents based on the functional groups present in its structure (e.g., piperidine, tetradecahydroanthracen-9-yl, and 1,2-dihydropyridine groups).

Solubility

The solubility of the compound in different solvents (e.g., water, organic solvents) would depend on the balance between its polar and nonpolar regions.

Stability

The stability of the compound under various conditions (e.g., temperature, pH, light exposure) would need to be determined through further research.

Synthesis

The synthesis of 1-[10-(piperidin-1-yl)tetradecahydroanthracen-9-yl]-1,2-dihydropyridine would likely involve multiple steps, including the formation of the piperidine, tetradecahydroanthracen-9-yl, and 1,2-dihydropyridine groups, followed by their connection.

Biological Activity

The compound's biological activity, including its interactions with biological targets (e.g., receptors, enzymes) and its pharmacokinetics (absorption, distribution, metabolism, and excretion), would need to be investigated through in vitro and in vivo studies.

Check Digit Verification of cas no

The CAS Registry Mumber 69282-16-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,2,8 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 69282-16:
(7*6)+(6*9)+(5*2)+(4*8)+(3*2)+(2*1)+(1*6)=152
152 % 10 = 2
So 69282-16-2 is a valid CAS Registry Number.

69282-16-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(10-pyridin-1-ium-1-yl-9,10-dihydroanthracen-9-yl)pyridin-1-ium,bromide

1.2 Other means of identification

Product number -
Other names -

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:69282-16-2 SDS

69282-16-2Relevant articles and documents

An Investigation of the Retro Diels-Alder Reaction as a Method for the Generation of Diatomic Sulfur

Gilchrist, Thomas L.,Wood, Jane E.

, p. 9 - 16 (2007/10/02)

The cyclic disulfides 2,3-dithiabicyclooct-5-ene 5, 1,4-dihydro-2,3-benzodithin 6 and hexahydro-5,8-epoxy-2,3-benzodithiin 7 have been prepared by oxidation of the corresponding dithiols.Each of these compounds has been subjected to vapour phase pyrolysis in order to determine whether a retro Diels-Alder reaction occurs, leading to the formation of diatomic sulfur (S2) and a diene.Compounds 5 and 7 both appeared to decompose in this way; in each case the expected diene was detected in the pyrolysate together with sulfur (S8).Attempts to intercept S2 and thus to obtain direct evidence for its formation were not successful.The benzodithiin 6 underwent an analogous loss of sulfur on vapour phase pyrolysis, but only as a minor reaction pathway, and this decomposition pathway was not detectable in solution pyrolyses.Solution pyrolysis of 6 in the presence of N-phenylmaleinimide gave N-phenyl-2,3-naphthalimide 21 in low yield. cis-Cyclopentene-3,5-dithiol 9 has also been prepared but no evidence could be obtained for the formation of disulfide 4 on oxidation.Reaction of the dithiol 9 with aldehydes and ketones in the presence of acids led to the formation of adducts (such as 12 and 13 from acetone) which were rapidly interconverted in acidic media.

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