1228184-79-9

Basic information

• Product Name: C₁₄H₈F₄N₆O₂
• Synonyms: C₁₄H₈F₄N₆O₂
• CAS NO: 1228184-79-9
• Molecular Weight: 368.25
• Mol File: 1228184-79-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₁₄H₈F₄N₆O₂(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₄H₈F₄N₆O₂(1228184-79-9)
• EPA Substance Registry System: C₁₄H₈F₄N₆O₂(1228184-79-9)

Safety Data

• Hazardous Substances Data: 1228184-79-9(Hazardous Substances Data)

Upstream product

• 675-14-9 trifluoro-[1,3,5]triazine 
• 626-18-6 1,3-dimethanol benzene 

Relevant articles and documents

Synthesis, structure, and functionalization of homo heterocalix[2]arene[2] triazines: Versatile conformation and cavity structures regulated by the bridging elements

Figure presented A number of homo[2] and homo[4] heterocalix[2]arene[2] triazines were synthesized through a general and good-yielding fragment coupling approach starting from cyanuric halides, aromatic and aliphatic diols, and diamines under very mild reaction conditions. While homo[2] tetraazacalix[2] arene[2]triazine gave a twisted and pinched 1,2-alternate conformer, almost all homo[2] heterocalix[2]arene[2]triazines adopted different partial cone conformations in the solid state. Homo[4] heterocalix[2]arene[2]triazines yielded more diverse conformational structures including partial cone, pinched partial cone, 1,2-alternate and twisted 1,2-alternate, depending on the nature of bridging moieties. On the basis of 1H NMR spectra, homo[2] and homo[4] heterocalix[2]arene[2]triazines were fluxional macrocycles in solution, and they underwent rapid conformation interconversion at different temperatures. Efficient and straightforward nucleophilic aromatic substitution reaction and palladium-catalyzed cross-coupling reactions on chlorotriazine rings, and the nucleophilic alkylation reaction on the bridging nitrogen atoms led to the construction of various highly functionalized homo heterocalix[2]arene[2] triazine derivatives.