45427-50-7

Basic information

• Product Name: 1,3,5-Triazine, 1,2-dihydro-
• CAS NO: 45427-50-7
• Molecular Formula: C3H5N3
• Molecular Weight: 83.0928
• Mol File: 45427-50-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1,3,5-Triazine, 1,2-dihydro-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,5-Triazine, 1,2-dihydro-(45427-50-7)
• EPA Substance Registry System: 1,3,5-Triazine, 1,2-dihydro-(45427-50-7)

Safety Data

• Hazardous Substances Data: 45427-50-7(Hazardous Substances Data)

Usage

General Description

1,3,5-Triazine, 1,2-dihydro- is a chemical compound with the chemical formula C3H6N4. It is a six-membered heterocyclic ring that contains three nitrogen atoms and three carbon atoms. 1,3,5-Triazine, 1,2-dihydro- is used as an intermediate in the synthesis of various organic chemicals and pharmaceuticals. It is also commonly used as a building block in the synthesis of various heterocyclic compounds, such as pyridazines and pyrimidines. Additionally, it can be used as a reagent in organic synthesis to create new compounds with specific chemical properties. Overall, 1,3,5-Triazine, 1,2-dihydro- has a wide range of applications in the chemical industry and organic synthesis.

Upstream product

• 290-87-9 1,3,5-Triazine 

Relevant articles and documents

Ru-Catalyzed Transfer Hydrogenation of Nitriles, Aromatics, Olefins, Alkynes and Esters

This paper reports the preparation of new ruthenium(II) complexes supported by a pyrazole-phosphine ligand and their application to transfer hydrogenation of various substrates. These Ru complexes were found to be efficient catalysts for the reduction of nitriles and olefins. Heterocyclic compounds undergo transfer hydrogenation with good to moderate yields, affording examples of unusual hydrogenation of all-carbon-rings. Internal alkynes with bulky substituents show selective reduction to olefins with the unusual E–selectivity. Esters with strong electron-withdrawing groups can be reduced to the corresponding alcohols, if ethanol is used as the solvent. Possible mechanisms of hydrogenation and olefin isomerization are suggested on the basis of kinetic studies and labelling experiments.

Process for the preparation of hydroxyphenyl-1,3,5-triazines

A simple process for the preparation of a triazine of formula (1) is described, which comprises converting a dihydrotriazine of formula (2) with a reducing agent to a 1,3,5-triazine of formula (1). The triazines obtained by the novel process are suitable UV absorbers for organic materials, in particular for polyester fiber materials, or suitable starting materials for the preparation of UV absorbers.