5660-43-5

Basic information

• Product Name: phenyl(1-prop-2-en-1-yl-1H-benzimidazol-2-yl)methanol
• Synonyms: (1-Allyl-1H-benzimidazol-2-yl)(phenyl)methanol; (1-Allyl-1H-benzoimidazol-2-yl)-phenyl-methanol; 1H-Benzimidazole-2-methanol, alpha-phenyl-1-(2-propen-1-yl)-
• CAS NO: 5660-43-5
• Molecular Formula: C₃₀H₂₂
• Molecular Weight: 264.3217
• Mol File: 5660-43-5.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 473.7°C at 760 mmHg
• Flash Point: 240.3°C
• Density: 1.13g/cm³
• Vapor Pressure: 8.9E-10mmHg at 25°C
• Refractive Index: 1.612
• CAS DataBase Reference: phenyl(1-prop-2-en-1-yl-1H-benzimidazol-2-yl)methanol(CAS DataBase Reference)
• NIST Chemistry Reference: phenyl(1-prop-2-en-1-yl-1H-benzimidazol-2-yl)methanol(5660-43-5)
• EPA Substance Registry System: phenyl(1-prop-2-en-1-yl-1H-benzimidazol-2-yl)methanol(5660-43-5)

Safety Data

• Hazardous Substances Data: 5660-43-5(Hazardous Substances Data)

Upstream product

• 615-42-9 1,2-Diiodobenzene 
• 1591-31-7 4-iodo-biphenyl 
• 24253-44-9 4,4''-diiodo-o-terphenyl 
• 71-43-2 benzene 
• 5122-94-1 4-biphenylboronic acid 
• 583-53-9 2,3-dibromobenzene 
• 822-87-7 2-Chlorocyclohexanone 
• 93902-63-7 2-(4-Xenyl)-cyclohexanol 
• 93877-01-1 2-((1,1'-biphenyl)-4-yl)cyclohexan-1-one 
• 92-66-0 4-bromo-1,1'-biphenyl 
• 96468-28-9 1,2-Di-(4-Xenyl)-cyclohexanol-⁽¹⁾ 
• 130951-97-2 4,4''-diamino-1,1',2',1''-terphenyl 

Downstream Products

• 24253-53-0 2,11-diphenyltriphenylene 

Relevant articles and documents

SINGLE TRIPHENYLENE CHROMOPHORES IN PHOSPHORESCENT LIGHT EMITTING DIODES

Novel triphenylene compounds are provided. Specific examples include multi-aryl-substituted triphenylenes. A preferred group of compounds are triphenylenes that are substituted with a non-fused aryl group having one or more meta-substituents, where each meta-substituent is a non-fused aryl group optionally substituted with further substituents selected from the group consisting of non-fused aryl groups and alkyl groups. A further preferred group of compounds are triphenylenes that are substituted with a non-fused heteroaryl group having one or more meta-substituents, where each meta-substituent is a non-fused aryl or heteroaryl group optionally substituted with further substituents selected from the group consisting of non-fused aryl groups, non-fused heteroaryl groups, and alkyl groups. Some high triplet energy analogs are expected to work with deep blue phosphorescent dopants. The compounds may be useful in phosphorescent organic light emitting devices. Also provided is an organic electroluminescent device comprising an anode, a cathode, and an emissive layer between the anode and the cathode, the emissive layer comprising a phosphorescent material and a compound having a repeat unit, the repeat unit containing a triphenylene moiety.