18028-56-3 Usage
General Description
1,4,6-trimethyl-9H-carbazole is a chemical compound with the molecular formula C16H15N. It is a heterocyclic organic compound that consists of a carbazole ring with three methyl groups attached at the 1, 4, and 6 positions. 1,4,6-trimethyl-9H-carbazole is a derivative of carbazole, which is commonly used in organic synthesis and has various industrial applications. 1,4,6-trimethyl-9H-carbazole is a pale yellow crystalline solid that is insoluble in water but soluble in organic solvents. It is used as a building block in the synthesis of dyes, pigments, and pharmaceuticals, and it also exhibits potential as a material for organic light-emitting diodes and hole transport materials in electronic devices. Additionally, it has been studied for its potential use as a corrosion inhibitor and an antioxidant. Overall, 1,4,6-trimethyl-9H-carbazole has versatile applications in industry and research.
Check Digit Verification of cas no
The CAS Registry Mumber 18028-56-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,0,2 and 8 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 18028-56:
(7*1)+(6*8)+(5*0)+(4*2)+(3*8)+(2*5)+(1*6)=103
103 % 10 = 3
So 18028-56-3 is a valid CAS Registry Number.
18028-56-3Relevant articles and documents
New trimethoxybenzamides and trimethoxyphenylureas derived from dimethylcarbazole as cytotoxic agents. Part i
Panno, Antonella,Sinicropi, Maria Stefania,Caruso, Anna,El-Kashef, Hussein,Lancelot, Jean-Charles,Aubert, Geneviève,Lesnard, Aurélien,Cresteil, Thierry,Rault, Sylvain
, p. E294-E302 (2014/11/08)
A convenient synthesis of novel functionalized 1,4-dimethylcarbazole derivatives containing 3,4,5-trimethoxybenzamido-ureido or N-(3,4,5- trimethoxyphenyl)ureido group starting from their corresponding indole derivatives is reported. Three derivatives pre
Solvent-free solid acid-catalyzed electrophilic annelations: A new green approach for the synthesis of substituted five-membered N-heterocycles
Abid, Mohammed,Spaeth, Andrew,Toeroek, Bela
, p. 2191 - 2196 (2007/10/03)
An effective microwave-induced, solid acid-catalyzed, environmentally benign synthesis of substituted pyrroles, indoles and carbazoles under solvent-free conditions is described. The new synthetic methodology is based on the use of a considerably strong solid acid, K-10 montmorillonite. Both the cyclialkylation of amines and annelation of pyrroles and indoles have been completed within minutes and provided excellent (75-98%) yields with practically 100% selectivity.