88368-24-5 Usage
Chemical class
Pyrimido[5,4-c]carbazole class of compounds
Structural features
Contains a chlorine atom and a methyl group
Type of compound
Heterocyclic compound
Potential applications
Biological and pharmaceutical applications
Studied properties
Anticancer and antiviral properties
Additional potential
Fluorescent dye for bioimaging and diagnosis
Research and development
Candidate for further research in medicine and materials science
Unique structure
Contributes to its potential in various fields
Molecular weight
Approximately 262.72 g/mol (calculated from the chemical formula)
Check Digit Verification of cas no
The CAS Registry Mumber 88368-24-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,3,6 and 8 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 88368-24:
(7*8)+(6*8)+(5*3)+(4*6)+(3*8)+(2*2)+(1*4)=175
175 % 10 = 5
So 88368-24-5 is a valid CAS Registry Number.
88368-24-5Relevant academic research and scientific papers
Synthese de Dihydro-6,7 5H-pyrimidinocarbazoles et de 7H-Pyrimidinocarbazoles
Lancelot, Jean-Charles,Gazengel, Jean-Marie,Robba, Max
, p. 2652 - 2661 (2007/10/02)
The synthesis of 6,7-dihydro-5H-pyrimidinocarbazoles (3) was achived by cyclisation of 1,2,3,4-tetrahydrocarbazol-4-ones with triformamidomethane.The oxydation with potassium permanganate of 6,7-dihydro-5H-pyrimidinocarbazoles gave the 7H-pyrimidinocarbazoles (4).The reactions of the pyrimidinocarbazoles (4a) and (4e) with lithium organic compounds afforded 4-substituted derivatives (6).The structure of the derivatives was determined by (1)H-NMR and Overhauser effect.Keywords - 1,2,3,4-tetrahydrocarbazol-4-one; 6,7-dihydro-5H-pyrimidinocarbazole; 7H-pyrimidinocarbazole; (1)H-NMR; Overhauser effect
