34049-45-1

Basic information

• Product Name: fluoranthen-8-ol
• Synonyms: 8-Fluoranthenol
• CAS NO: 34049-45-1
• Molecular Formula: C₁₆H₁₀O
• Molecular Weight: 218.25
• Mol File: 34049-45-1.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 437.4°C at 760 mmHg
• Flash Point: 213°C
• Density: 1.36g/cm³
• Vapor Pressure: 2.92E-08mmHg at 25°C
• Refractive Index: 1.895
• CAS DataBase Reference: fluoranthen-8-ol(CAS DataBase Reference)
• NIST Chemistry Reference: fluoranthen-8-ol(34049-45-1)
• EPA Substance Registry System: fluoranthen-8-ol(34049-45-1)

Safety Data

• Hazardous Substances Data: 34049-45-1(Hazardous Substances Data)

Upstream product

• 206-44-0 fluoranthene 
• 79870-17-0 8-oxo-6b,7,8,9,10,10a-hexahydrofluoranthene 
• 58485-91-9 6b,7,10,10a-tetrahydrofluoranthene 
• 79870-16-9 8-hydroxy-6b,7,8,9,10,10a-hexahydrofluoranthene 

Relevant articles and documents

Metal Arene Complexes in Organic Synthesis. Hydroxylation, Trimethylsilylation, and Carbethoxylation of Some Polycyclic Aromatic Hydrocarbons Utilizing η6-Arene-Chromium Tricarbonyl Complexes

The deprotonation of polycyclic aromatic hydrocarbon (PAH) chromium tricarbonyl complexes (PAH = naphthalene, anthracene, phenanthrene, pyrene, fluoranthene) using an in situ technique where the PAH complex, the base (LiTMP or LDA), and the electrophile (trialkyl borate, trimethylsilyl chloride, or ethyl chloroformate) were placed in solution simultaneously resulted in hydroxylation, trimethylsilylation, or carbethoxylation of the PAH after oxidative workup where the regiochemistry was controlled by steric factors.As a result, substitution at positions of the PAHs not readily available by electrophilic substitution were obtained in some cases.Conditions minimizing isomer mixtures and factors affecting the regiochemistry and the scope of the reaction sequence were examined.