42880-08-0

Basic information

• Product Name: 2-(2,4-DIMETHOXYSTYRYL)-4,6-BIS(TRICHLOROMETHYL)-1,3,5-TRIAZINE
• Synonyms: 2-(2,4-DIMETHOXYSTYRYL)-4,6-BIS(TRICHLOROMETHYL)-1,3,5-TRIAZINE;4,6-bis-(trichloromethyl)-2-(2,4-Dimethoxystyryl)-1,3,5-Triazine
• CAS NO: 42880-08-0
• Molecular Formula: C15H11Cl6N3O2
• Molecular Weight: 477.98
• Mol File: 42880-08-0.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(2,4-DIMETHOXYSTYRYL)-4,6-BIS(TRICHLOROMETHYL)-1,3,5-TRIAZINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2,4-DIMETHOXYSTYRYL)-4,6-BIS(TRICHLOROMETHYL)-1,3,5-TRIAZINE(42880-08-0)
• EPA Substance Registry System: 2-(2,4-DIMETHOXYSTYRYL)-4,6-BIS(TRICHLOROMETHYL)-1,3,5-TRIAZINE(42880-08-0)

Safety Data

• Hazardous Substances Data: 42880-08-0(Hazardous Substances Data)

Usage

General Description

2-(2,4-DIMETHOXYSTYRYL)-4,6-BIS(TRICHLOROMETHYL)-1,3,5-TRIAZINE is a chemical compound with a molecular formula C21H18Cl6N4O2. It is a triazine derivative that contains trichloromethyl and dimethoxystyryl groups. 2-(2,4-DIMETHOXYSTYRYL)-4,6-BIS(TRICHLOROMETHYL)-1,3,5-TRIAZINE is a potential inhibitor of the enzyme aldose reductase, which is involved in the development of diabetic complications. Additionally, it has been studied for its potential anti-tumor properties, with research suggesting that it may inhibit the growth of certain cancer cells. Further investigation is needed to fully understand the pharmacological and toxicological properties of this compound.

Relevant articles and documents

Process for preparing chromophore-substituted vinyl-halomethyl-s-triazines

An improved method for the preparation of chromophore-substituted vinyl-halomethyl-s-triazines especially 2-(p-methoxystyryl)-4,6-bis-(trichloromethyl)-s-triazine. In the known preparation of these compounds, a two step procedure is utilized wherein an intermediate reaction product has to be isolated. This step of separating the intermediate is eliminated in the present process by dissolving the crude reaction product obtained in the first step in toluene, removing excess hydrogen chloride gas and catalysts by purging the reaction product solution with an inert gas, and then reacting p-anisaldehyde with the toluene solution of the reaction product mixture using piperidinium acetate catalyst to obtain 2-(p-methoxystyryl)-4,6-bis-(trichloromethyl)-s-triazine. As a further improvement of the art the Knoevenagel-type condensation is run until no further water is evolved. At this point the product formed is isolated by filtration and a like amount of catalyst as a second charge is added. Again, the reaction is carried out until no further water is evolved and further product is isolated by filtration.