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Atomfair 1H-Imidazole, 2-(2-chlorophenyl)-1-[2-(2-chlorophenyl)-4,5-diphenyl-2H-imidazol-2-yl]-4,5-diphenyl- C42H28Cl2N4 CAS 7189-82-4
1H-Imidazole, 2-(2-chlorophenyl)-1-[2-(2-chlorophenyl)-4,5-diphenyl-2H-imidazol-2-yl]-4,5-diphenyl- (CAS No. 7189-82-4) is a high-purity biimidazole derivative with the molecular formula C42H28Cl2N4. This specialized organic compound features a complex imidazole core structure substituted with chlorophenyl and phenyl groups, making it a valuable reagent for advanced chemical synthesis and materials research. Its unique steric and electronic properties are ideal for applications in photochemistry, coordination chemistry, and as a potential ligand or building block for functional materials. Available in research-grade purity, this compound is meticulously characterized by NMR, HPLC, and mass spectrometry to ensure consistency and reliability for demanding laboratory applications.
Description
1H-Imidazole, 2-(2-chlorophenyl)-1-[2-(2-chlorophenyl)-4,5-diphenyl-2H-imidazol-2-yl]-4,5-diphenyl- (CAS No. 7189-82-4) is a high-purity biimidazole derivative with the molecular formula C42H28Cl2N4. This specialized organic compound features a complex imidazole core structure substituted with chlorophenyl and phenyl groups, making it a valuable reagent for advanced chemical synthesis and materials research. Its unique steric and electronic properties are ideal for applications in photochemistry, coordination chemistry, and as a potential ligand or building block for functional materials. Available in research-grade purity, this compound is meticulously characterized by NMR, HPLC, and mass spectrometry to ensure consistency and reliability for demanding laboratory applications.
Properties
- CAS Number: 7189-82-4
- Complexity: 1080
- IUPAC Name: 2-(2-chlorophenyl)-1-[2-(2-chlorophenyl)-4,5-diphenyl-imidazol-2-yl]-4,5-diphenyl-imidazole
- InChI: InChI=1S/C42H28Cl2N4/c43-35-27-15-13-25-33(35)41-45-39(31-21-9-3-10-22-31)40(32-23-11-4-12-24-32)48(41)42(34-26-14-16-28-36(34)44)46-37(29-17-5-1-6-18-29)38(47-42)30-19-7-2-8-20-30/h1-28H
- InChI Key: MHDULSOPQSUKBQ-UHFFFAOYSA-N
- Exact Mass: 658.1691023
- Molecular Formula: C42H28Cl2N4
- Molecular Weight: 659.6
- SMILES: C1=CC=C(C=C1)C2=C(N(C(=N2)C3=CC=CC=C3Cl)C4(N=C(C(=N4)C5=CC=CC=C5)C6=CC=CC=C6)C7=CC=CC=C7Cl)C8=CC=CC=C8
- Topological: 42.5
- Monoisotopic Mass: 658.1691023
- Synonyms: 7189-82-4, 2,2′-Bis(2-chlorophenyl)-4,4′,5,5′-tetraphenyl-1,2′-biimidazole, 1H-Imidazole, 2-(2-chlorophenyl)-1-[2-(2-chlorophenyl)-4,5-diphenyl-2H-imidazol-2-yl]-4,5-diphenyl-, EINECS 230-555-6, DTXSID5074929, 1H-Imidazole, 2-(2-chlorophenyl)-1-(2-(2-chlorophenyl)-4,5-diphenyl-2H-imidazol-2-yl)-4,5-diphenyl-, 2-(2-Chlorophenyl)-1-(2-(2-chlorophenyl)-4,5-diphenyl-2H-imidazol-2-yl)-4,5-diphenyl-1H-imidazole, 2-(2-chlorophenyl)-1-[2-(2-chlorophenyl)-4,5-diphenyl-2H-imidazol-2-yl]-4,5-diphenyl-1H-imidazole, DTXCID1047156, 230-555-6, 2,2′-bis(2-chlorophenyl)-4,4′,5,5′-tetraphenyl-2’h-1,2′-biimidazole, 2,2-Bis(2-chlorophenyl)-4,4,5,5-tetraphenyl-1,2-biimidazole, MFCD09028023, 2-(2-chlorophenyl)-1-[2-(2-chlorophenyl)-4,5-diphenylimidazol-2-yl]-4,5-diphenylimidazole, 2,2′-Bis(2-chlorophenyl)-4,4’5,5′-tetraphenyl-1,2′-biimidazole, 6143-80-2, C42H28Cl2N4, SCHEMBL307038, AKOS015896133, AC-16733, AS-17693, SY053318, B1225, CS-0373828, NS00037301, D97685, 2,2′-bis(o-chlorophenyl)-4,4′,5,5′-tetraphenyl-1,2′-biimidazole, 2,2′-Bis(2-dichlorophenyl)-4,4’5,5′-tetraphenyl-1,2′-biimidazole, 2,2′-Bis(o-chlorophenyl)-4,4′,5,5′-tetraphenyl-1,2′-bi(iii-imidazole), 2,2′-Bis(2-chlorophenyl)-4,4′,5,5′-tetraphenyl-1,2′-biimidazole, 2,2 inverted exclamation mark -Bis(2-chlorophenyl)-4,4 inverted exclamation mark ,5,5 inverted exclamation mark -tetraphenyl-2 inverted exclamation mark H-1,2 inverted exclamation mark -biimidazole
This compound is primarily used as a photopolymerization initiator in advanced materials science, particularly in UV-curable coatings and adhesives. Its bifunctional imidazole structure makes it suitable for studying electron-transfer processes in photochemical systems. Researchers also employ it as a ligand precursor in coordination chemistry for designing novel metal-organic frameworks (MOFs) or catalysts. Additionally, its extended conjugated system may be explored for optoelectronic applications.
Safety and Hazards
GHS Hazard Statements
- Not Classified
- Reported as not meeting GHS hazard criteria by 70 of 71 companies (only 1.4% companies provided GHS information). For more detailed information, please visit ECHA C&L website.
Hazard Classes and Categories
- Not Classified
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Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.
Disclaimer
Intended Use & Restrictions
This product is sold exclusively for laboratory research, analytical testing, or non-commercial purposes.
- Strictly prohibited: Resale, repackaging, or formulation into commercial products.
- Not approved for human/animal use, diagnostics, or manufacturing (including pharmaceuticals, agrochemicals, or consumer goods).
Patent & Regulatory Compliance
Certain molecules may be protected by active patents or regulatory restrictions.
- Buyers must independently verify patent status (e.g., via USPTO/EPO/CNIPA) and comply with local laws.
- Atomfair LLC does not provide legal assurances regarding patent non-infringement or jurisdictional compliance.
Liability Release
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- Use this product only as permitted by law.
- Indemnify Atomfair LLC against all claims arising from misuse, patent infringement, or regulatory violations.
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