60432-61-3 Usage
Chemical Family
Belongs to the indole family, which is a group of organic compounds containing an indole ring.
Molecular Structure
Bicyclic organic compound with a unique indenoindole structure, which consists of two fused rings (indole and indene).
Functional Group
Contains a phenyl group, which is an aromatic ring with six carbon atoms and six hydrogen atoms.
Applications
Has potential applications in medicinal chemistry and drug discovery due to its pharmacological activities.
Pharmacological Activities
Exhibits anti-cancer, anti-inflammatory, and anti-microbial properties, making it a promising candidate for further research and drug development.
Research Interest
Its complex structure and diverse biological activities make it an interesting molecule for scientists to study and explore its potential uses.
Potential Drug Development
Due to its pharmacological properties, 10-phenyl-5,10-dihydroindeno[1,2-b]indole may be considered for the development of new drugs targeting various diseases and conditions.
Molecular Weight
The molecular weight of 10-phenyl-5,10-dihydroindeno[1,2-b]indole is approximately 283.35 g/mol.
Solubility
The solubility of 10-phenyl-5,10-dihydroindeno[1,2-b]indole may vary depending on the solvent used, but it is generally more soluble in organic solvents like ethanol, methanol, or dimethyl sulfoxide (DMSO).
Check Digit Verification of cas no
The CAS Registry Mumber 60432-61-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,4,3 and 2 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 60432-61:
(7*6)+(6*0)+(5*4)+(4*3)+(3*2)+(2*6)+(1*1)=93
93 % 10 = 3
So 60432-61-3 is a valid CAS Registry Number.
60432-61-3Relevant academic research and scientific papers
Pyrolysis of quinoline-3,4-dicarboxylic anhydrides bearing 2-phenyl, 2-benzyl and 2-o-tolyl substituents: Formation of products of carbene insertion and addition
Brown,Coulston,Eastwood,Moffat
, p. 7763 - 7774 (2007/10/02)
Flash vacuum pyrolysis of 2-phenylquinoline-3,4-dicarboxylic anhydride at 800°/0.06 mm gave indeno[1,2-b]indole (30-40%), which readily added nucleophiles Y- at C-10 to give 5,10-dihydro derivatives (Y=H, Me, Ph, NEt2, OMe, CH(COOMe)2 and CMe2NO2). Similar pyrolysis of the 2-benzylquinoline anhydride gave a 1:2 mixture of the (expected) linear 5H-benzo[b]carbazole and the (unexpected) angular 7H-benzo[c]carbazole. The isomeric 2-o-tolylquinoline anhydride on similar pyrolysis gave mainly 11H-benzo[a]carbazole (85%), isomeric benzocarbazoles (4%) and 11H-indeno[1,2-b]quinoline (2.6%). Most of these products are probably derived from exocyclic carbenes formed by aryne-carbene equilibration, but the last compound may be formed by direct aryne-methyl interaction.
Synthesis of indeno[1,2-b]indole by flash vacuum pyrolysis of 2-phenylquinoline-3,4-dicarboxylic anhydride
Brown,Coulston,Eastwood,Moffat
, p. 801 - 802 (2007/10/02)
Flash vacuum pyrolysis of 2-phenylquinoline-3,4-dicarboxylic anhydride at 800°C/0.06 Torr. gave indenol[1,2-b]indole. This was reduced to form 5,10-dihydroindenol[1,2-b]indole and it added nucleophiles to give dihydroindenoindoles with the 10-substituents
