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

General Description

2,4,6-Tris(4-ethynylphenyl)-1,3,5-triazine is a complex organic chemical compound known for its unique structure involving a triazine ring substituted with three 4-ethynylphenyl groups. Given its specialized nature, it's often included in high-level chemistry studies and applications, including pharmaceutical research or advanced material science. The precise properties of this compound, such as its boiling/melting point, density or solubility, may vary depending on the specific synthesis process, but in general it requires stringent and controlled conditions to handle and store properly due to its reactivity. More detailed information on this chemical can be found in material safety data sheets and scientific literature.

Upstream product

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

Downstream Products

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

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