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Sigma-Aldrich

2-Phenylimidazol

98%

Synonym(e):

2-Phenyl-1H-imidazole

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About This Item

Empirische Formel (Hill-System):
C9H8N2
CAS-Nummer:
670-96-2
Molekulargewicht:
144.17
EG-Nummer:
211-581-7
MDL-Nummer:
MFCD00005186
UNSPSC-Code:
12352005
PubChem Substanz-ID:
24853589
NACRES:
NA.22

Assay

98%

Form

solid

mp (Schmelzpunkt)

142-148 °C (lit.)

SMILES String

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)

InChIKey

ZCUJYXPAKHMBAZ-UHFFFAOYSA-N

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Anwendung

2-Phenylimidazole was used to prepare complex compounds with ruthenium(III).

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

H-Sätze

H302

Gefahreneinstufungen

Acute Tox. 4 Oral

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

392.0 °F

Flammpunkt (°C)

200 °C

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves

Analysenzertifikate (COA)

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Sigma-Aldrich

369713

1-Benzyl-2-methylimidazol

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Sigma-Aldrich

278289

1-Phenylpyrazol

1-Butylimidazol 98%

Sigma-Aldrich

348414

1-Butylimidazol

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.
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
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).
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
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