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224,000+ productos de investigación · Triple ISO certified · COA & SDS Disponible para cada producto · 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 Sinónimos
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
Especificaciones y pureza
≥98%
Condiciones de almacenamiento de almacenamiento
Room temperature
Nombres e identificadores Pubchem Sid 504754413 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504754413 Sonrisas canónicas 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) Isómeros SMILES C1=CC=C(C=C1)C2=C(N=CN2)C3=CC=CC=C3 WGK Alemania 3 Peso molecular 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 Clase 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 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.
Estructura 3D Objetivos asociados (humanos) Objetivos asociados (no humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Solubilidad Soluble in methanol. Punto de fusión (°C) 230°C Peso molecular 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 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. 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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