2,4,6-Triphenyl-1,3,5-triazine (purified by sublimation) - ≥99% , CAS No.493-77-6

CAS: 493-77-6 Cat. No.: T162547 Peso molecular: 309.37 Número EC: 207-779-8 PubChem CID: 10305

GRADE & PURITY ≥99%

Synonyms

FT-0632226 | 1,5-Triazine, 2,4,6-triphenyl- | s-Triazine,4,6-triphenyl- | AI3-61032 | 2,6-Triphenyl-s-triazine | AMY37878 | triphenyl-1,3,5-triazine | NSC46521 | NSC-46521 | T2785 | 1,3,5-Triazine, 2,4,6-triphenyl- | 2,4,6-Triphenyl-1,3,5-triazine | AS-48

Storage

Room temperature

Shipped In

Normal

Descripción general

Hole blocking capability of 2,4,6-triphenyl-1,3,5-triazine as a non-transporting filler material has been investigated.

Specifications

Sinónimos

FT-0632226 | 1, 5-Triazine, 2, 4, 6-triphenyl- | s-Triazine, 4, 6-triphenyl- | AI3-61032 | 2, 6-Triphenyl-s-triazine | AMY37878 | triphenyl-1, 3, 5-triazine | NSC46521 | NSC-46521 | T2785 | 1, 3, 5-Triazine, 2, 4, 6-triphenyl- | 2, 4, 6-Triphenyl-1, 3, 5-triazine | AS-48

Especificaciones y pureza

≥99%

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Pureza

≥99%

Nombres e identificadores

• Pubchem Sid: 488181111
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488181111
• Sonrisas canónicas: C1=CC=C(C=C1)C2=NC(=NC(=N2)C3=CC=CC=C3)C4=CC=CC=C4
• IUPAC Name: 2,4,6-triphenyl-1,3,5-triazine
• InChIKey: HBQUOLGAXBYZGR-UHFFFAOYSA-N
• INCHI: 1S/C21H15N3/c1-4-10-16(11-5-1)19-22-20(17-12-6-2-7-13-17)24-21(23-19)18-14-8-3-9-15-18/h1-15H
• Isómeros SMILES: C1=CC=C(C=C1)C2=NC(=NC(=N2)C3=CC=CC=C3)C4=CC=CC=C4
• WGK Alemania: 3
• PubChem CID: 10305
• Peso molecular: 309.37
• Reaxy-Rn: 239186

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Clase Triazines
      • Subclass 1,3,5-triazines

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Clase: Triazines
• Subclass: 1,3,5-triazines
• Intermediate Tree Nodes: Not available
• Direct Parent: 1,3,5-triazines
• Alternative Parents: Benzene and substituted derivatives Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: 1,3,5-triazine - Benzenoid - Monocyclic benzene moiety - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteromonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as 1,3,5-triazines. These are compounds containing a triazine ring, which is a heterocyclic ring, similar to the six-member benzene ring but with three carbons replaced by nitrogen atoms, at ring positions 1, 3, and 5.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Propiedades químicas y físicas

• Punto de ebullición (°C): 230°C/0.01mmHg(lit.)
• Punto de fusión (°C): 236 °C
• Peso molecular: 309.400 g/mol
• XLogP3: 5.000
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 309.127 Da
• Monoisotopic Mass: 309.127 Da
• Topological Polar Surface Area: 38.700 Ų
• Heavy Atom Count: 24
• Formal Charge: 0
• Complexity: 298.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Referencias

1. Yafang Zhang, Pengfei Hua, Yanfu Chai, Yujing Zuo.  (2024)  Versatile organosilicone porous materials for the detection of nitroaromatics and the visualization of fingerprints.  EUROPEAN POLYMER JOURNAL,      [PMID:] [10.1016/j.eurpolymj.2024.113576]

2. Xiaofeng Li, Zimo Wang, Yaohan Chen, Yonggang Li, Jing Guo, Jifu Zheng, Shenghai Li, Suobo Zhang.  (2023)  Imidazolium-based AEMs with high dimensional and alkaline-resistance stabilities for extended temperature range of alkaline fuel cells.  JOURNAL OF MEMBRANE SCIENCE,      [PMID:] [10.1016/j.memsci.2023.121352]