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224,000+ research products · Triple ISO certified · COA & SDS available for every product · Same-day shipping on in-stock items 4,5-Diphenylimidazole - ≥98% , CAS No.668-94-0
Synonyms
SCHEMBL16503669 | 1H-Imidazole,5-diphenyl- | 4,5-diphenyl imidazole | 4,5-Diphenyl-1H-imidazole # | Tox21_110979_1 | D2107 | DTXCID3025700 | AC-907/25014326 | 4,5-Diphenylimidazole, 98% | A835576 | FT-0617216 | US9144538, 4,5-diphenylimidazole | InChI=1/C
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Why this grade ≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Room temperature Ships Normal Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 3 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Synonyms
SCHEMBL16503669 | 1H-Imidazole, 5-diphenyl- | 4, 5-diphenyl imidazole | 4, 5-Diphenyl-1H-imidazole # | Tox21_110979_1 | D2107 | DTXCID3025700 | AC-907/25014326 | 4, 5-Diphenylimidazole, 98% | A835576 | FT-0617216 | US9144538, 4, 5-diphenylimidazole | InChI=1/C
Specifications & Purity
≥98%
Names and Identifiers Pubchem Sid 504754413 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504754413 Canonical Smiles C1=CC=C(C=C1)C2=C(N=CN2)C3=CC=CC=C3 IUPAC Name 4,5-diphenyl-1H-imidazole InChIKey CPHGOBGXZQKCKI-UHFFFAOYSA-N INCHI 1S/C15H12N2/c1-3-7-12(8-4-1)14-15(17-11-16-14)13-9-5-2-6-10-13/h1-11H,(H,16,17) Isomeric SMILES C1=CC=C(C=C1)C2=C(N=CN2)C3=CC=CC=C3 WGK Germany 3 Molecular Weight 220.27 Beilstein 23(3/4)1812 Reaxy-Rn 157587 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=157587&ln=
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Organoheterocyclic compounds Class Azoles Subclass Imidazoles Intermediate Tree Nodes Substituted imidazoles Direct Parent Phenylimidazoles Alternative Parents Benzene and substituted derivatives Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives Molecular Framework Aromatic heteromonocyclic compounds Substituents 4-phenylimidazole - 5-phenylimidazole - Benzenoid - Monocyclic benzene moiety - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteromonocyclic compound Description 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.
3D Structure Associated Targets(Human) Associated Targets(non-human) Mechanisms of Action Certificates(CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Solubility Soluble in methanol. Melt Point(°C) 230°C Molecular Weight 220.270 g/mol XLogP3 3.400 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 1 Rotatable Bond Count 2 Exact Mass 220.1 Da Monoisotopic Mass 220.1 Da Topological Polar Surface Area 28.700 Ų Heavy Atom Count 17 Formal Charge 0 Complexity 229.000 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
Citations of This Product References 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. Yafei Sang, Zhe Shu, You Wang, Lizhi Wang, Du Zhang, Qin Xiao, Fa Zhou, Jianhan Huang. (2022) Bifunctional ionic hyper-cross-linked polymers for CO2 capture and catalytic conversion. APPLIED SURFACE SCIENCE, [PMID: ] [10.1016/j.apsusc.2022.152663 ] 3. Hong Yang, Ming Xu, Ling-Xiang Guo, Hao-Fan Ji, Jun-Yu Wang, Bao-Ping Lin, Xue-Qin Zhang, Ying Sun. (2014) Organocatalysis in polysiloxane gels: a magnetic-stir-bar encapsulated catalyst system prepared by thiol–ene photo-click immobilization. RSC Advances, 5 (10): (7304-7310). [PMID: ] [10.1039/C4RA16351F ]
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