Fluoronaphthalene Basic information
Product Name: Fluoronaphthalene
Synonyms: 1-Fluornaftalen;1-fluoro-naphthalen;alpha-Fluoronaphthalene;1-FLUORONAPHTHALENE;1-FLUORONAPTHALENE;Fluoronaphthalene;1-FLUORONAPHTHALENE, 1000MG, NEAT;I-Fluoronaphthalene
CAS: 321-38-0
MF: C10H7F
MW: 146.16
EINECS: 206-287-0
Product Categories: Other fluorin-contained compounds;Miscellaneous;Alpha Sort;E-LAlphabetic;F;FA - FLChemical Class;FluoroAnalytical Standards;Naphthalenes;Volatiles/ Semivolatiles;Method 625EPA;600 Series Wastewater Methods;8000 Series Solidwaste Methods;Chemical Class;FluoroEPA;Halogenated;Method 8100;Aryl;C9 to C12;Halogenated Hydrocarbons;Aromatics;Impurities;Intermediates & Fine Chemicals;Pharmaceuticals;Fluorine series;Aromatics, Impurities, Pharmaceuticals, Intermediates & Fine Chemicals
Mol File: 321-38-0.mol
Fluoronaphthalene Structure
Fluoronaphthalene Chemical Properties
Melting point −13 °C(lit.)
Boiling point 215 °C(lit.)
density 1.1322 g/mL at 20 °C(lit.)
refractive index n20/D 1.593(lit.)
Fp 150 °F
storage temp. room temp
Water Solubility Not miscible or difficult to mix in water.
BRN 1906413
Stability: Stable. Incompatible with strong oxidizing agents.
CAS DataBase Reference 321-38-0(CAS DataBase Reference)
NIST Chemistry Reference Naphthalene, 1-fluoro-(321-38-0)
EPA Substance Registry System Naphthalene, 1-fluoro-(321-38-0)
Safety Information
Hazard Codes Xi,F,T,Xn
Risk Statements 36/37/38-63-43-23/24/25-45-40
Safety Statements 26-36-36/37-24/25-23-53
RIDADR UN 2810
WGK Germany 3
RTECS QJ7100000
Hazard Note Flammable
TSCA T
HazardClass IRRITANT
MSDS Information
Provider Language
Fluoronaphthalene English
SigmaAldrich English
ACROS English
ALFA English
Fluoronaphthalene Usage And Synthesis
Chemical Properties clear slightly yellow to yellow-brown liquid
Uses A fluorinated naphthalene derivative that is metabolized by fungal monooxygenase-epoxide hydrolase. Duloxetine (D721000) impurity.
General Description Needles.
Air & Water Reactions Insoluble in water.
Reactivity Profile Simple aromatic halogenated organic compounds, such as Fluoronaphthalene, are very unreactive. Reactivity generally decreases with increased degree of substitution of halogen for hydrogen atoms. Materials in this group may be incompatible with strong oxidizing and reducing agents. Also, they may be incompatible with many amines, nitrides, azo/diazo compounds, alkali metals, and epoxides.
Fluoronaphthalene Preparation Products And Raw materials
Preparation Products 4-Fluoronaphtalene-1-boronic acid-->2-(1-FLUORONAPHTHALEN-4-YL)-4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLANE-->Duloxetine