62732-44-9 Usage
Description
2,3,5,6,7,8-HEXAHYDRO-1H-CYCLOPENTA[B]QUINOLIN-9-YLAMINE is a complex organic compound with a unique molecular structure. It is characterized by its hexahydrocyclopentafused quinoline core and an amine functional group at the 9-position. 2,3,5,6,7,8-HEXAHYDRO-1H-CYCLOPENTA[B]QUINOLIN-9-YLAMINE has potential applications in various fields due to its unique chemical properties and interactions with biological systems.
Uses
Used in Pharmaceutical Industry:
2,3,5,6,7,8-HEXAHYDRO-1H-CYCLOPENTA[B]QUINOLIN-9-YLAMINE is used as a potential therapeutic agent for the treatment of toxic cognitive disorders. Its unique molecular structure allows it to interact with specific biological targets, potentially modulating the underlying mechanisms of these disorders and providing relief to affected individuals.
Used in Biological Studies:
In the field of biological research, 2,3,5,6,7,8-HEXAHYDRO-1H-CYCLOPENTA[B]QUINOLIN-9-YLAMINE serves as a valuable tool for studying the molecular mechanisms underlying various cognitive and neurological conditions. Its interactions with biological systems can provide insights into the development of novel therapeutic strategies and help researchers better understand the complex processes involved in these disorders.
Check Digit Verification of cas no
The CAS Registry Mumber 62732-44-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,7,3 and 2 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 62732-44:
(7*6)+(6*2)+(5*7)+(4*3)+(3*2)+(2*4)+(1*4)=119
119 % 10 = 9
So 62732-44-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H16N2/c13-12-8-4-1-2-6-10(8)14-11-7-3-5-9(11)12/h1-7H2,(H2,13,14)
62732-44-9Relevant articles and documents
Process for the preparation of ipidacrine or ipidacrine hydrochloride hydrate
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, (2008/06/13)
A process for the preparation of ipidacrine (I) (9-amino-2,3,5,6,7,8-hexahydro-1H-cyclopenta[b]quinoline) which comprises the reaction of diphosphorus pentaoxide with a trialkyl phosphate and a hydroxyl compound in a hydrocarbon solvent to thereby prepare a polyphosphoric ester having one or more free hydroxyl groups and serving as a dehydrocondensing agent and using this ester without isolation in the condensation of 2-amino-1-cyclopentene-1-carbonitrile with cyclohexanone through dehydration.
Recyclization of 2,2-Disubstituted 4(3H)-Oxo- and 4-Chloro-1,2-dihydropyrimidines to 4-Aminopyridine Derivatives
Upadysheva, A. V.,Grigor'eva, N. D.,Ryabokobylko, Yu. S.,Znamenskaya, A. P.
, p. 95 - 99 (2007/10/02)
The intramolecular cationotropic rearrangement of salts of two-ring 2,2-disubstituted 4-chloro-1,2-dihydropyrimidines to 4-aminopyrimidine derivatives was observed.Recyclization to 4-aminopyridines can take place in the reaction of two-ring 2,2-disubstituted 4(3H)-oxo-1,2-dihydropyrimidines with phosphorus oxychloride without isolation of the intermediate chloro derivatives.A probable mechanism that makes it possible to assert that the observed recyclization is a variant of the intramolecular cationotropic rearrangement that is characteristic for 2,2-dialkylsubstituted 1,2-dihydropyrimidines with functional substituents (for example, oxo or chloro) in the 4 position of the ring is discussed.