87019-98-5

Basic information

• Product Name: 2,4,6-tris[(E)-2-phenylethenyl]-1,3,5-triazine
• Synonyms: 2,4,6-tris[(E)-2-phenylethenyl]-1,3,5-triazine
• CAS NO: 87019-98-5
• Molecular Weight: 387.484
• Mol File: 87019-98-5.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 2,4,6-tris[(E)-2-phenylethenyl]-1,3,5-triazine(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4,6-tris[(E)-2-phenylethenyl]-1,3,5-triazine(87019-98-5)
• EPA Substance Registry System: 2,4,6-tris[(E)-2-phenylethenyl]-1,3,5-triazine(87019-98-5)

Safety Data

• Hazardous Substances Data: 87019-98-5(Hazardous Substances Data)

Upstream product

• 823-94-9 2,4,6-trimethyl-s-triazine 
• 100-46-9 benzylamine 
• 108-77-0 1,3,5-trichloro-2,4,6-triazine 
• 201852-49-5 potassium (E)-trifluoro(styryl)borate 
• 100-52-7 benzaldehyde 
• 949-42-8 2,4-bis(trichloromethyl)-6-methyl-1,3,5-triazine 
• 6783-05-7 trans-2-phenylvinylboronic acid 
• 1885-38-7 cinnamic nitrile 
• 333-27-7 methyl trifluoromethanesulfonate 
• 4360-47-8 cinnamonitrile 
• 1493-13-6 trifluorormethanesulfonic acid 

Relevant articles and documents

Deaminative Olefination of Methyl N-Heteroarenes by an Amine Oxidase Inspired Catalyst

We explored the bioinspired o-quinone cofactor catalyzed aerobic primary amine dehydrogenation for a cascade olefination reaction with nine different methyl N-heteroarenes, including pyrimidines, pyrazines, pyridines, quinolines, quinoxolines, benzimidazoles, benzoxazoles, benzthiazoles, and triazines. An o-quinone catalyst phd (1,10-phenanthroline-5,6-dione) combined with a Br?nsted acid catalyzed the reaction. N-Heteroaryl stilbenoids were synthesized in high yields and (E)-selectivities under mild conditions using oxygen (1 atm) as the sole oxidant without needing transition-metal salt, ligand, stoichiometric base, or oxidant.

Porous Crystalline Olefin-Linked Covalent Organic Frameworks

The first unsubstituted olefin-linked covalent organic framework, termed COF-701, was made by linking 2,4,6-trimethyl-1,3,5-triazine (TMT) and 4,4′-biphenyldicarbaldehyde (BPDA) through Aldol condensation. Formation of the unsubstituted olefin (-CHa?CH-)

Suzuki-Miyaura cross-coupling reactions of potassium alkenyltrifluoroborates

We have previously reported that the palladium-catalyzed cross-coupling reaction of air-stable potassium alkenyltrifluoroborates with aryl halides and triflates proceeds readily with good yields. Recent progress in outlining the scope and limitations of s