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1-Fluoronaphthalene

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Identification
Molecular formula
C10H7F
CAS number
321-38-0
IUPAC name
1-fluoronaphthalene
State
State

At room temperature, 1-Fluoronaphthalene is a liquid state. It is commonly handled under standard laboratory conditions.

Melting point (Celsius)
-32.00
Melting point (Kelvin)
241.15
Boiling point (Celsius)
204.00
Boiling point (Kelvin)
477.00
General information
Molecular weight
146.16g/mol
Molar mass
146.1600g/mol
Density
1.1440g/cm3
Appearence

1-Fluoronaphthalene appears as a clear, colorless liquid. It is often used in chemical research and as an intermediate in organic synthesis.

Comment on solubility

Solubility of 1-Fluoronaphthalene

1-Fluoronaphthalene, with the chemical formula C10H7F, exhibits unique solubility characteristics that can be quite interesting:

  • Polarities: Being a fluorinated aromatic compound, 1-fluoronaphthalene is less polar than many other compounds due to the presence of the fluorine atom, which can influence its interactions with solvents.
  • Solvent Compatibility: It is generally soluble in organic solvents such as hexane, benzene, and ether, but shows limited solubility in water due to its hydrophobic naphthalene structure.
  • Temperature Dependence: The solubility may vary with temperature; higher temperatures often increase solubility in organic solvents as kinetic energy allows for better interaction and dissolution.
  • Applications: The solubility properties of 1-fluoronaphthalene make it useful in various applications, including organic synthesis and as a solvent in specific chemical reactions.

In summary, 1-fluoronaphthalene's solubility highlights the behavior of fluorinated compounds, showcasing their affinity for non-polar organic solvents while exhibiting resistance to polar environments like water.

Interesting facts

1-Fluoronaphthalene: A Fascinating Organic Compound

1-Fluoronaphthalene is an intriguing aromatic compound that showcases the unique properties of halogenated naphthalenes. As a member of the naphthalene family, it consists of two fused benzene rings, combined with a single fluorine atom attached to one of the positions. Here are some captivating facts about this compound:

  • Functional Representation: The introduction of the fluorine atom significantly alters the compound's chemical reactivity and physical properties compared to its parent naphthalene.
  • Applications: 1-Fluoronaphthalene serves as a valuable intermediate in the synthesis of various chemicals. It is often used in the production of pharmaceuticals, agrochemicals, and in the development of fluorinated materials.
  • Insight into Halogen Chemistry: Studying this compound is essential for chemists interested in halogenation reactions, as the presence of fluorine in organic molecules can lead to significant enhancements in biological activity.
  • Physical Properties: Despite being a trifluoromethyl compound, 1-fluoronaphthalene displays unique characteristics such as non-polarity, which might impact its behavior in various solvent systems.
  • Cultural Significance: Like other fluorinated compounds, 1-fluoronaphthalene has sparked interest in eco-toxicology, making it relevant in discussions on the environmental impact of synthetic chemicals.

The exploration and application of 1-fluoronaphthalene exemplify the intersection of organic chemistry with practical applications in industry and environmental science. It poses profound questions about sustainability and the future of halogenated compounds in our rapidly evolving chemical landscape.

Synonyms
1-FLUORONAPHTHALENE
321-38-0
Fluoronaphthalene
Naphthalene, 1-fluoro-
alpha-Fluoronaphthalene
1-Fluornaftalen
.alpha.-Fluoronaphthalene
1-Fluornaftalen [Czech]
NSC 4690
EINECS 206-287-0
BRN 1906413
1-fluoranylnaphthalene
Duloxetine IMpurity G
UNII-0920702UT7
NSC-4690
MFCD00003873
0920702UT7
DTXSID7059808
4-05-00-01657 (Beilstein Handbook Reference)
DULOXETINE IMPURITY G [USP IMPURITY]
1-fluoro naphthalene
DULOXETINE HYDROCHLORIDE IMPURITY G [EP IMPURITY]
DULOXETINE IMPURITY G (USP IMPURITY)
DULOXETINE HYDROCHLORIDE IMPURITY G (EP IMPURITY)
fluoronaphtalene
fluoronapthalene
1Fluornaftalen
1-fluoronapthalene
1-fluoro-naphtalene
1-fluoro-naphthalene
alphaFluoronaphthalene
Fluoronaphthalene, 1
Naphthalene, 1fluoro
A-FLUORONAPHTHALENE
1-Fluoronaphthalene, 99%
WLN: L66J BF
SCHEMBL151748
DTXCID1038454
NSC4690
1-Fluoronaphthalene 2000 microg/mL in Methyl-tert-butyl ether
BCP11223
AKOS005257808
CCG-321350
IF23445
AC-17493
AC-31039
AS-12061
HY-32126
DB-291392
CS-0001469
F0212
NS00042293
EN300-73626
A25262
NSC 4690;a-Fluoronaphthalene;Duloxetine impurity G
Q18923301
Z1162445957
2-bromo-naphthalen;2-Naphthyl bromide;Naphthalene, 2-bromo-;naphthalene,2-bromo-
206-287-0
Y84