2,4,5-Triphenylimidazole - ≥98% , CAS No.484-47-9

CAS: 484-47-9 Cat. No.: T138898 Peso molecular: 296.37 Beilstein Registry Number: 236652 Número EC: 207-606-6 PubChem CID: 10232

GRADE & PURITY ≥98%

Synonyms

DTXSID3022039 | CCRIS 8668 | SR-01000510787-2 | T0999 | Q6K46G80ZD | 2,5-Triphenylimidazole | SCHEMBL104130 | 2,4,5-Triphenyl-1H-imidazole | A827535 | EINECS 207-606-6 | SR-01000510787 | NCI60_008969 | EN300-1661101 | Lophin | 2,4,5-Triphenylimidazole, 98

Storage

Room temperature

Shipped In

Normal

Descripción general

application：

2,4,5-Triphenylimidazole is used in the synthesis of fluorescent diarylethenes and nanowires of 2,4,5-triphenylimidazole, which finds application as single wire active optical waveguides and optically driven ultraviolet lasers.

Specifications

Sinónimos

DTXSID3022039 | CCRIS 8668 | SR-01000510787-2 | T0999 | Q6K46G80ZD | 2, 5-Triphenylimidazole | SCHEMBL104130 | 2, 4, 5-Triphenyl-1H-imidazole | A827535 | EINECS 207-606-6 | SR-01000510787 | NCI60_008969 | EN300-1661101 | Lophin | 2, 4, 5-Triphenylimidazole, 98

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 488181093
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488181093
• Sonrisas canónicas: C1=CC=C(C=C1)C2=C(N=C(N2)C3=CC=CC=C3)C4=CC=CC=C4
• IUPAC Name: 2,4,5-triphenyl-1H-imidazole
• InChIKey: RNIPJYFZGXJSDD-UHFFFAOYSA-N
• INCHI: 1S/C21H16N2/c1-4-10-16(11-5-1)19-20(17-12-6-2-7-13-17)23-21(22-19)18-14-8-3-9-15-18/h1-15H,(H,22,23)
• Isómeros SMILES: C1=CC=C(C=C1)C2=C(N=C(N2)C3=CC=CC=C3)C4=CC=CC=C4
• PubChem CID: 10232
• Peso molecular: 296.37
• Beilstein: 236652

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Clase Azoles
      • Subclass Imidazoles
        • Level5 Substituted imidazoles
          • Level6 Phenylimidazoles

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Clase: Azoles
• Subclass: Imidazoles
• Intermediate Tree Nodes: Substituted imidazoles
• Direct Parent: Phenylimidazoles
• Alternative Parents: 2,4,5-trisubstituted imidazoles Benzene and substituted derivatives Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: 4-phenylimidazole - 5-phenylimidazole - 2-phenylimidazole - Trisubstituted imidazole - 2,4,5-trisubstituted-imidazole - 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 phenylimidazoles. These are polycyclic aromatic compounds containing a benzene ring linked to an imidazole ring through a CC or CN bond.
• 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

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ACHE Tclin Acetylcholinesterase (18204 Activities)

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Soat1 Acyl coenzyme A:cholesterol acyltransferase 1 (295 Activities)

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Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Soluble in methanol. Insoluble in water.
• Punto de fusión (°C): 275 °C
• Peso molecular: 296.400 g/mol
• XLogP3: 5.000
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 3
• Exact Mass: 296.131 Da
• Monoisotopic Mass: 296.131 Da
• Topological Polar Surface Area: 28.700 Ų
• Heavy Atom Count: 23
• Formal Charge: 0
• Complexity: 351.000
• 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. Mingming Xu, Zhijun Zhou, Lin Hao, Zhi Li, Jie Li, Qianqian Wang, Weihua Liu, Chun Wang, Zhi Wang, Qiuhua Wu.  (2022)  Phenyl-imidazole based and nitrogen rich hyper-crosslinked polymer for sensitive determination of aflatoxins.  FOOD CHEMISTRY,      [PMID:] [10.1016/j.foodchem.2022.134847]

2. Zhizhou Liu, Chao Li, Chen Chen, Tong Wang, Liang He, Xueyan Nan, Li Li, Qing Qian, Pengli Bai.  (2022)  The danger of dichloromethane in the synthesis and application of imidazole-based dyes.  DYES AND PIGMENTS,      [PMID:] [10.1016/j.dyepig.2022.110404]

3. Hai Li, Yang You, Chun Hui Xie, Yun Qi Li, Hai Bo Xie.  (2024)  High-Performance Adhesive with Wide Working Temperature Range Enabled by the Multivalent Supramolecular Network around Lignin-Derived Noncoplanar Triaryl-imidazolium.  MACROMOLECULES,      [PMID:] [10.1021/acs.macromol.4c02402]