375365
4-Methyl-2-phenylimidazole
95%
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About This Item
Empirical Formula (Hill Notation):
C10H10N2
CAS Number:
Molecular Weight:
158.20
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
212-571-5
MDL number:
Assay:
95%
InChI key
TYOXIFXYEIILLY-UHFFFAOYSA-N
InChI
1S/C10H10N2/c1-8-7-11-10(12-8)9-5-3-2-4-6-9/h2-7H,1H3,(H,11,12)
SMILES string
Cc1c[nH]c(n1)-c2ccccc2
assay
95%
mp
180-183 °C (lit.)
General description
4-Methyl-2-phenylimidazole is a 4-substituted-2-phenylimidazole. It participates in ring-opening of various bicyclic olefins to afford trans-3,4-disubstituted derivatives. The FT-IR, FT-Raman and FT-NMR spectra of 4-methyl-2-phenylimidazole has been recorded.
Application
4-Methyl-2-phenylimidazole is suitable for use to investgate the cytotoxic activity of 4-trifluoromethylimidazoles against human tumor and normal cells. It may be used in following studies:
- Curing of epoxy system consisting of a diglycidyl ether of bisphenol-F epoxy resin, 1,4-butanediol.
- Curing of bisphenol-F epoxy resin.
- Synthesis of aza-heterocyclic compounds.
- Preparation of 1-[(2-chlorophenyl)(diphenyl)methyl]-4-methyl-2-phenyl-1H-imidazole.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Theoretical investigations on the molecular structure and vibrational spectral analysis of 4-methyl 2-phenylimidazole.
Erdogdu Y, et al.
Optics and Spectroscopy, 113(6), 596-606 (2012)
Rhodium (III)-catalyzed CH activation of phenylazoles toward CN bond cleavage of diazabicyclic olefins: A facile access to mono-and biscyclopentenyl-functionalized aza-heteroaromatics
Praveen P, et al.
Synlett, 25, 0275-0279 (2014)
Fumihiro Takekawa et al.
Anticancer research, 27(6B), 4065-4069 (2008-01-30)
Fourteen 4-trifluoromethylimidazole derivatives were investigated for their cytotoxicity against three human normal cells (gingival fibroblast HGF, pulp cell HPC and periodontal ligament fibroblast HPLF) and four human tumor cell lines (oral squamous cell carcinoma HSC-2, HSC-3, HSC-4 and promyelocytic leukemia
Cure profiles, crosslink density, residual stresses, and adhesion in a model epoxy.
Case SL, et al.
Polymer, 46(24), 1083-1040 (2005)
Physical properties of a bisphenol-F epoxy containing a silica filler treated with silane coupling agents.
Case SL and Ward TC.
Journal of Adhesion, 79(2), 105-121 (2003)
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