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226769

Sigma-Aldrich

2-Phenylimidazole

98%

Sinonimo/i:

2-Phenyl-1H-imidazole

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About This Item

Formula empirica (notazione di Hill):
C9H8N2
Numero CAS:
670-96-2
Peso molecolare:
144.17
Numero CE:
211-581-7
Numero MDL:
MFCD00005186
Codice UNSPSC:
12352005
ID PubChem:
24853589
NACRES:
NA.22

Saggio

98%

Forma fisica

solid

Punto di fusione

142-148 °C (lit.)

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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Categorie correlate

Applicazioni

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

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H302

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

Certificati d'analisi (COA)

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Sigma-Aldrich

369713

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Sigma-Aldrich

278289

1-Phenylpyrazole

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Sigma-Aldrich

348414

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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
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
T Shimizu et al.
Biochimica et biophysica acta, 995(2), 116-121 (1989-04-06)
By site-directed mutagenesis, we made several cytochrome P-450d (P-450d) mutants as follows: Asn310Phe (D13), Ile312Leu (D14), Glu318Asp (D15), Val320Ile (D16), Phe325Thr (D19), Asn310Phe,Ile312Leu (M6), Glu318Asp,Val320Ile (M7), Phe325Thr, Glu318Asp (M3). This region (Asn-310-Phe-325) is supposed to be located in the distal
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