91544-98-8 Usage
Molecular structure
1-methyl-3-(4-methylbenzoyl)-9H-carbazole-2-carboxylic acid consists of a carbazole ring with a methyl group at position 1, a 4-methylbenzoyl group at position 3, and a carboxylic acid group at position 2.
Classification
It is a derivative of carbazole, which is a heterocyclic aromatic organic compound, and specifically classified as a carboxylic acid.
Functional groups
The compound contains a methyl group (-CH3), a 4-methylbenzoyl group (a benzoyl group with a methyl group attached to the benzene ring), and a carboxylic acid group (-COOH).
Potential applications
Due to its unique structure and properties, 1-methyl-3-(4-methylbenzoyl)-9H-carbazole-2-carboxylic acid has potential applications in the fields of organic synthesis, material science, pharmaceuticals, organic light-emitting diodes (OLEDs), and other electronic devices.
Chemical modifications
The specific chemical structure of the compound allows for the modification and manipulation of its properties for various industrial and research purposes.
Check Digit Verification of cas no
The CAS Registry Mumber 91544-98-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,5,4 and 4 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 91544-98:
(7*9)+(6*1)+(5*5)+(4*4)+(3*4)+(2*9)+(1*8)=148
148 % 10 = 8
So 91544-98-8 is a valid CAS Registry Number.
91544-98-8Relevant academic research and scientific papers
Pyridazinocarbazole: Synthese et Etude des Spectres de Resonance Magnetique Nucleaire
Lancelot, Jean-Charles,Landelle, Henriette,Robba, Max
, p. 902 - 908 (2007/10/02)
The acid anhydrides (5-7) were obtained by treatment of corresponding 2,3-carbazole-dicarboxylic acids (2-4) with acetic anhydride.Friedel-Crafts reaction of these anhydrides with benzene or toluole gave either 3-aroylcarbazole-2-carboxylic acids (8-11) o
