226769
2-Phenylimidazole
98%
Sinonimo/i:
2-Phenyl-1H-imidazole
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Informazioni su questo articolo
Formula empirica (notazione di Hill):
C9H8N2
Numero CAS:
Peso molecolare:
144.17
Numero CE:
Numero MDL:
Codice UNSPSC:
12352005
ID PubChem:
NACRES:
NA.22
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Permettici di aiutartiSaggio
98%
Stato
solid
Punto di fusione
142-148 °C (lit.)
Gruppo funzionale
phenyl
Stringa SMILE
c1ccc(cc1)-c2ncc[nH]2
InChI
1S/C9H8N2/c1-2-4-8(5-3-1)9-10-6-7-11-9/h1-7H,(H,10,11)
ZCUJYXPAKHMBAZ-UHFFFAOYSA-N
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Questo articolo | D208604 | H50802 | 232858 |
|---|---|---|---|
| assay 98% | assay 98% | assay 98% | assay 98% |
| Quality Level 200 | Quality Level 200 | Quality Level 100 | Quality Level 100 |
| form solid | form - | form - | form - |
| mp 142-148 °C (lit.) | mp 228-230 °C (lit.) | mp 122-124 °C (lit.) | mp 99-100 °C (lit.) |
| functional group phenyl | functional group - | functional group - | functional group hydroxyl |
Applicazioni
2-Phenylimidazole was used to prepare complex compounds with ruthenium(III)[1].
Avvertenze
Warning
Indicazioni di pericolo
Consigli di prudenza
Classi di pericolo
Acute Tox. 4 Oral
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
392.0 °F
Punto d’infiammabilità (°C)
200 °C
Dispositivi di protezione individuale
dust mask type N95 (US), Eyeshields, Gloves
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A Nikolova et al.
Arzneimittel-Forschung, 51(9), 758-762 (2001-10-20)
Complex compounds of ruthenium(III) with 1,2-dimethylimidazole (CAS 1739-84-0), 2-phenylimidazole (CAS 670-96-2) and 2-aminobenzimidazole (CAS 934-32-7) were prepared and were characterised by physicochemical methods. Coordination sites were determined. The complexes were tested for cytotoxic activity using MTT (3-(4,5-dimethyithiazol-2-yl)-2,5-diphenyltetrazolium bromide) dye-reduction assay
Manoj Kumar Dalai et al.
Indian journal of biochemistry & biophysics, 43(2), 105-118 (2006-09-08)
Considering the potential of peripheral benzodiazepine receptor (PBR) ligands in therapeutic applications and clinical benefit in the management of a large spectrum of different indications, quantitative structure-activity relationship (QSAR) study has been attempted to explore the structural and physicochemical requirements
Hyun Jung Koo et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 130, 99-108 (2019-05-22)
The aim of the present study was to investigate the detoxifying effects of aloe polysaccharide (APS), propolis, and the mixture of APS and propolis on the urinary excretion of major human tobacco carcinogens, BaP and an addictive stimulant alkaloid, nicotine.
T Shimizu et al.
Biochemistry, 30(6), 1490-1496 (1991-02-12)
Interactions of various axial ligands with cytochrome P-450d wild type, proximal mutants (Lys453Glu, Ile460Ser), and putative distal mutants (Glu318Asp, Thr319Ala, Thr322Ala) expressed in yeast were studied with optical absorption spectroscopy. P-450d wild type and all five mutants were purified essentially
Lourdes Infantes et al.
The journal of physical chemistry. A, 110(7), 2535-2544 (2006-02-17)
The enthalpies of combustion, heat capacities, enthalpies of sublimation and enthalpies of formation of 2-tert-butylbenzimidazole (2tBuBIM) and 2-phenylimidazole (2PhIM) are reported and the results compared with those of benzene derivatives and a series of azoles (imidazoles, pyrazoles, benzimidazoles and indazoles).
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