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18028-56-3

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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.

18028-56-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4,6-trimethyl-9H-carbazole

1.2 Other means of identification

Product number -
Other names 9H-Carbazole,1,4,6-trimethyl

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:18028-56-3 SDS

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.

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