425629-22-7

Basic information

• Product Name: 2,4,6-Tris(4-ethynylphenyl)-1,3,5-triazine
• Synonyms: 2,4,6-Tris(4-ethynylphenyl)-1,3,5-triazine
• CAS NO: 425629-22-7
• Molecular Formula: C₂₇H₁₅N₃
• Molecular Weight: 381.43
• Mol File: 425629-22-7.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 593.6±60.0 °C(Predicted)
• Appearance: /
• Density: 1.28±0.1 g/cm3(Predicted)
• PKA: 0.02±0.10(Predicted)
• CAS DataBase Reference: 2,4,6-Tris(4-ethynylphenyl)-1,3,5-triazine(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4,6-Tris(4-ethynylphenyl)-1,3,5-triazine(425629-22-7)
• EPA Substance Registry System: 2,4,6-Tris(4-ethynylphenyl)-1,3,5-triazine(425629-22-7)

Safety Data

• Hazardous Substances Data: 425629-22-7(Hazardous Substances Data)

Usage

Description

2,4,6-Tris(4-ethynylphenyl)-1,3,5-triazine is a complex organic chemical compound characterized by a triazine ring with three 4-ethynylphenyl groups attached. It is known for its unique structure and is typically involved in advanced chemistry studies and applications, such as pharmaceutical research and material science. 2,4,6-Tris(4-ethynylphenyl)-1,3,5-triazine's properties, including boiling/melting point, density, and solubility, can vary based on the synthesis process and require controlled conditions for handling and storage due to its reactivity.

Uses

Used in Pharmaceutical Research:
2,4,6-Tris(4-ethynylphenyl)-1,3,5-triazine is used as a research compound for its potential applications in the development of new pharmaceuticals. Its unique structure and reactivity make it a candidate for exploring novel drug interactions and mechanisms.
Used in Advanced Material Science:
In the field of material science, 2,4,6-Tris(4-ethynylphenyl)-1,3,5-triazine is utilized as a component in the synthesis of advanced materials with specific properties. Its ethynylphenyl groups and triazine ring can contribute to the creation of materials with tailored characteristics for various high-tech applications.

Upstream product

• 30363-03-2 2,4,6-tris(4-bromophenyl)-1,3,5-triazine 

Downstream Products

• 6091-44-7 piperidine hydrochloride 
• 1418421-63-2 2,4,6-[4-(Cl(PEt₃)₂PtCC)C₆H₄]₃-1,3,5-C₃N₃ 

Relevant articles and documents

Substituted 1,3,5-triazine hexacarboxylates as potential linkers for MOFs

Hexacarboxylates are promising linkers for MOFs such as NU-109 or NU-110, which possess large values for surfaces and pore volumina. Starting from 2,4,6-tris(bromoaryl)-1,3,5-triazines, palladium-catalyzed cross coupling reactions (Suzuki-Miyaura, Sonogas

Fluorescent Sulphur- and Nitrogen-Containing Porous Polymers with Tuneable Donor–Acceptor Domains for Light-Driven Hydrogen Evolution

Light-driven water splitting is a potential source of abundant, clean energy, yet efficient charge-separation and size and position of the bandgap in heterogeneous photocatalysts are challenging to predict and design. Synthetic attempts to tune the bandgap of polymer photocatalysts classically rely on variations of the sizes of their π-conjugated domains. However, only donor–acceptor dyads hold the key to prevent undesired electron-hole recombination within the catalyst via efficient charge separation. Building on our previous success in incorporating electron-donating, sulphur-containing linkers and electron-withdrawing, triazine (C3N3) units into porous polymers, we report the synthesis of six visible-light-active, triazine-based polymers with a high heteroatom-content of S and N that photocatalytically generate H2 from water: up to 915 μmol h?1 g?1 with Pt co-catalyst, and—as one of the highest to-date reported values ?200 μmol h?1 g?1 without. The highly modular Sonogashira–Hagihara cross-coupling reaction we employ, enables a systematic study of mixed (S, N, C) and (N, C)-only polymer systems. Our results highlight that photocatalytic water-splitting does not only require an ideal optical bandgap of ≈2.2 eV, but that the choice of donor–acceptor motifs profoundly impacts charge-transfer and catalytic activity.

Twinned Growth of Metal-Free, Triazine-Based Photocatalyst Films as Mixed-Dimensional (2D/3D) van der Waals Heterostructures

Design and synthesis of ordered, metal-free layered materials is intrinsically difficult due to the limitations of vapor deposition processes that are used in their making. Mixed-dimensional (2D/3D) metal-free van der Waals (vdW) heterostructures based on