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375365

4-Methyl-2-phenylimidazole

Name: 4-Methyl-2-phenylimidazole
Brand: ALDRICH

95%

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About This Item

Empirical Formula (Hill Notation):

C₁₀H₁₀N₂

CAS Number:

827-43-0

Molecular Weight:

158.20

NACRES:

NA.22

PubChem Substance ID:

24863384

UNSPSC Code:

12352100

EC Number:

212-571-5

MDL number:

MFCD00047015

Assay:

95%

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Properties

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

Description

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.

pictograms

GHS07

signalword

Warning

hcodes

H315,H319,H335

pcodes

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

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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Certificates of Analysis (COA)

Lot/Batch Number

03311DY

13317AQ

01812DU

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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

Praveen P, et al.

Synlett, 25, 0275-0279 (2014)

Tumor-specific cytotoxic activity and type of cell death induced by 4-trifluoromethylimidazoles in human oral squamous cell carcinoma cell lines.

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)

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Global Trade Item Number

SKU	GTIN
375365-25G	04061831834987