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About This Item
Empirical Formula (Hill Notation):
C10H10N2
CAS Number:
Molecular Weight:
158.20
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
95%
mp
180-183 °C (lit.)
SMILES string
Cc1c[nH]c(n1)-c2ccccc2
InChI
1S/C10H10N2/c1-8-7-11-10(12-8)9-5-3-2-4-6-9/h2-7H,1H3,(H,11,12)
InChI key
TYOXIFXYEIILLY-UHFFFAOYSA-N
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.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Rhodium (III)-catalyzed CH activation of phenylazoles toward CN bond cleavage of diazabicyclic olefins: A facile access to mono-and biscyclopentenyl-functionalized aza-heteroaromatics
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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)
Cure profiles, crosslink density, residual stresses, and adhesion in a model epoxy.
Case SL, et al.
Polymer, 46(24), 1083-1040 (2005)
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)
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
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