5983-45-9 Usage
General Description
The chemical "5H-Imidazo[2,1-a]isoindol-5-one, 9b-(4-chlorophenyl)-1-ethyl-1,2,3,9b-tetrahydro-" is a compound with a complex molecular structure. It is a derivative of imidazoisoindole, with an ethyl and chlorophenyl group attached to it. This chemical is classified as a heterocyclic compound, containing nitrogen atoms in its ring structure. The presence of the chlorophenyl group indicates that 5H-Imidazo[2,1-a]isoindol-5-one,
9b-(4-chlorophenyl)-1-ethyl-1,2,3,9b-tetrahydro- is likely to have specific pharmacological or biological activities, and it may be used in pharmaceutical research or drug development. The tetrahydro structure suggests that it may have potential as a psychoactive substance, although further research is needed to fully understand its properties and potential applications.
Check Digit Verification of cas no
The CAS Registry Mumber 5983-45-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,8 and 3 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5983-45:
(6*5)+(5*9)+(4*8)+(3*3)+(2*4)+(1*5)=129
129 % 10 = 9
So 5983-45-9 is a valid CAS Registry Number.
5983-45-9Relevant academic research and scientific papers
Polycyclic amino derivatives of pyrrolidone and piperidone
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, (2008/06/13)
A series of compounds of the formula STR1 have been found to exhibit useful pharmacological properties, e.g. antiinflammatory and analgetic activity.
5H-imidazo[2,1-a]isoindol-5-one compounds
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, (2008/06/13)
A new class of chemical compounds whose members exert an appetite suppressant and mood elevating effect in man has been invented. This class is defined as being composed of those compounds having the 1-substituted-2,5-benzodiazocine structure, fully saturated in the nonbenzenoid portion, and whose nitrogens are tervalent. Members of this class are prepared by condensing an orthobenzoylbenzoic acid or ester thereof with an ethylenediamine and reducing with a metallic alkaline hydride the product thus obtained.
