7651-80-1

Basic information

• Product Name: 1-FLUOROANTHRACENE
• Synonyms: 1-FLUOROANTHRACENE
• CAS NO: 7651-80-1
• Molecular Formula: C14H9F
• Molecular Weight: 196.22
• Mol File: 7651-80-1.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 341℃
• Flash Point: 130℃
• Appearance: /
• Density: 1.212
• Refractive Index: 1.5678 (estimate)
• Water Solubility: 0.26mg/L(temperature not stated)
• CAS DataBase Reference: 1-FLUOROANTHRACENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-FLUOROANTHRACENE(7651-80-1)
• EPA Substance Registry System: 1-FLUOROANTHRACENE(7651-80-1)

Safety Data

• Hazardous Substances Data: 7651-80-1(Hazardous Substances Data)

Usage

Chemical Structure

1-Fluoroanthracene is a polycyclic aromatic hydrocarbon (PAH) with a central anthracene ring and a fluorine atom attached to one of its carbon atoms.

Physical State

It is a colorless solid.

Organic Synthesis

1-Fluoroanthracene is used in the synthesis of various organic compounds.

Fluorescent Probe

It is used as a fluorescent probe in biochemical and pharmaceutical research.

Insoluble in Water

1-Fluoroanthracene does not dissolve in water.

Soluble in Organic Solvents

It dissolves in organic solvents like alcohol, ether, and acetone.

Melting Point

1-Fluoroanthracene has a high melting point.

Persistence

It is a potential environmental pollutant due to its persistence in the environment.

Toxicity

It has potential toxicity to aquatic organisms.

Safety Precautions

It is important to handle and dispose of 1-Fluoroanthracene safely to minimize its impact on human health and the environment.

Upstream product

• 610-49-1 1-aminoanthracene 
• 569-06-2 1-fluoro-9,10-anthraquinone 
• 82-44-0 1-chloroanthracene-9,10-dione 
• 7397-92-4 1-bromoanthracene 
• 133745-75-2 N-fluorobis(benzenesulfon)imide 
• 82-45-1 1-amino-9,10-anthracenedione 
• 82-37-1 9,10-dioxo-9,10-dihydroanthracene-1-diazonium hydrogen sulfate 
• 1121-86-4 1-Fluoro-3-iodobenzene 
• 529-20-4 2-methylphenyl aldehyde 
• 591-50-4 iodobenzene 
• 117752-04-2 2-fluoro-6-methylbenzaldehyde 

Downstream Products

• 569-06-2 1-fluoro-9,10-anthraquinone 
• 216-00-2 dibenzo[a,c]naphthacene 
• 54458-84-3 1-methoxyanthracene 

Relevant articles and documents

Cascade reaction for the synthesis of polycyclic aromatic hydrocarbons via transient directing group strategy

A Pd(II)-catalyzed cascade synthesis of diverse polycyclic aromatic hydrocarbons via transient directing group strategy has been developed, involving the consecutive arylation, cyclization and aromatization. The efficiency and practicality were demonstrated by wide substrate range, concise synthetic pathway and mild reaction conditions. The subsequent transformations of the benz[a]anthracene core accessed natural bioactive PAH molecules.

Aluminium-mediated aromatic C-F bond activation: Regioswitchable construction of benzene-fused triphenylene frameworks

Selective synthesis of benzo[f]tetraphenes or benzo[g]chrysenes was achieved via aromatic C-F bond cleavage and unprecedented regioselective C-C bond formation depending upon the choice of aluminium reagents. On treatment with AlCl3, 2-(bipheny

N-fluorosulfonimides and their application as fluorinating agents

The invention describes N-fluorosulfonimides which are useful as fluorinating agents. The N-fluorosulfonimides are stable, easily synthesized, and allow the introduction of fluorine into organic compounds under mild conditions.