1919-48-8 Usage
Description
2,4,6-Triphenoxy-1,3,5-triazine is an organic compound characterized by its unique triazine ring structure with three phenoxy groups attached at the 2, 4, and 6 positions. It is an off-white to light beige fluffy powder, which contributes to its distinct chemical properties and potential applications in various fields.
Uses
Used in Polymer Science:
2,4,6-Triphenoxy-1,3,5-triazine is used as a key component in the study of steric structure effects within the triazine system. This research is crucial for understanding the formation of polymeric structures and their properties, which can lead to the development of new materials with improved characteristics.
Used in Chemical Research:
As an organic compound with a triazine ring and phenoxy substituents, 2,4,6-Triphenoxy-1,3,5-triazine is utilized in chemical research to explore its reactivity, stability, and potential interactions with other molecules. This can contribute to the discovery of new chemical reactions and the synthesis of novel compounds with specific properties.
Used in Pharmaceutical and Agrochemical Industries:
Given its unique structure and chemical properties, 2,4,6-Triphenoxy-1,3,5-triazine may have potential applications in the pharmaceutical and agrochemical industries. It could be used as a building block for the development of new drugs or agrochemicals, or as an intermediate in the synthesis of various organic compounds.
Used in Material Science:
The properties of 2,4,6-Triphenoxy-1,3,5-triazine, such as its off-white to light beige fluffy powder form, make it a candidate for use in material science. It could be incorporated into the development of new materials with specific characteristics, such as improved thermal stability, mechanical strength, or optical properties.
Check Digit Verification of cas no
The CAS Registry Mumber 1919-48-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,1 and 9 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1919-48:
(6*1)+(5*9)+(4*1)+(3*9)+(2*4)+(1*8)=98
98 % 10 = 8
So 1919-48-8 is a valid CAS Registry Number.
InChI:InChI=1/C21H15N3O3/c1-4-10-16(11-5-1)25-19-22-20(26-17-12-6-2-7-13-17)24-21(23-19)27-18-14-8-3-9-15-18/h1-15H
1919-48-8Relevant articles and documents
-
Gibson,Murray
, p. 880 (1965)
-
Nickel-catalyzed reductive amidation of aryl-triazine ethers
Heravi, Majid M.,Panahi, Farhad,Iranpoor, Nasser
supporting information, p. 1992 - 1995 (2020/02/22)
The reaction of activated phenolic compounds, 2,4,6-triaryloxy-1,3,5-triazine (aryl-triazine ethers), with various isocyanates or carbodiimides in the presence of a nickel pre-catalyst resulted in the synthesis of aryl amides in good to excellent yields.
Choline Hydroxide as a Versatile Medium for Catalyst-Free O-Functionalization of Phenols
Joo, Seong-Ryu,Kim, Seung-Hoi,Kwon, Gyu-Tae,Park, Soo-Youl
, p. 1200 - 1205 (2020/11/30)
A versatile synthetic protocol for benzyl phenyl ether preparation via O-alkylation of phenolic oxygen with readily available benzyl derivatives was demonstrated. The newly designed procedure was carried out using an eco-friendly medium, room-temperature ionic liquid (choline hydroxide), under metal- and base-catalyst-free aerobic conditions. The reaction platform was also successfully applied to phenol protection strategy.
