Skip to main content

3-Fluoroanisole

ADVERTISEMENT
Identification
Molecular formula
C7H7FO
CAS number
456-49-5
IUPAC name
1-fluoro-3-methoxy-benzene
State
State

3-Fluoroanisole is in a liquid state at room temperature. It is typically handled and stored in its liquid form.

Melting point (Celsius)
-47.00
Melting point (Kelvin)
226.15
Boiling point (Celsius)
160.00
Boiling point (Kelvin)
433.15
General information
Molecular weight
126.13g/mol
Molar mass
126.1300g/mol
Density
1.1160g/cm3
Appearence

3-Fluoroanisole is a clear, colorless liquid. It has a distinctive anisole-like aromatic odor.

Comment on solubility

Solubility of 1-fluoro-3-methoxy-benzene

1-fluoro-3-methoxy-benzene, also known as m-fluoroanisole, exhibits notable solubility characteristics which are influenced by its functional groups. Understanding the solubility of this compound allows for insights into its behavior in various solvents:

  • Polar Solvents: 1-fluoro-3-methoxy-benzene shows moderate solubility in polar solvents such as water, due to its methoxy group which can interact through hydrogen bonding to some extent.
  • Non-Polar Solvents: This compound is more soluble in non-polar solvents like hexane or benzene. The non-polar aromatic ring enhances its ability to dissolve in similar non-polar environments.
  • Solubility Trends: As a general trend, compounds like 1-fluoro-3-methoxy-benzene tend to be more soluble in solvents that can effectively interact with their functional groups.

In summary, when considering the solubility of 1-fluoro-3-methoxy-benzene:

  1. Expect greater solubility in non-polar solvents.
  2. Moderate solubility can be anticipated in polar solvents.

These interactions underscore the importance of molecular structure in determining solubility behavior in analytical and industrial applications.

Interesting facts

Interesting Facts about 1-Fluoro-3-methoxy-benzene

1-Fluoro-3-methoxy-benzene, commonly known as fluoromethoxybenzene, is a fascinating organic compound with a variety of applications and unique chemical properties. Here are some engaging facts about this compound:

  • Structural Significance: The presence of both a fluorine atom and a methoxy group on the benzene ring significantly influences its reactivity, making it an intriguing focus for synthetic chemists.
  • Influence of Fluorine: The fluorine substituent is known for its strong electronegativity. This affects the compound's overall polarity and can enhance its biological activity, resulting in interesting interactions in various chemical reactions.
  • Versatile Synthesis: This compound can be synthesized through various methods, notably via nucleophilic aromatic substitution, where the methoxy group can serve as a leaving group.
  • Applications in Industry: 1-Fluoro-3-methoxy-benzene finds applications in the production of pharmaceuticals and agrochemicals, showcasing the importance of small modifications in organic synthesis.
  • Role in Material Science: Due to its chemical characteristics, it can also be utilized in the development of advanced materials and polymers, demonstrating the versatility of fluoro-substituted aromatics.

As a compound that bridges the gap between everyday applications and advanced research, 1-fluoro-3-methoxy-benzene illustrates how nuanced modifications in chemical structure can lead to significant changes in behavior and utility. Its study continues to contribute to the growing field of organic chemistry.

Synonyms
3-Fluoroanisole
456-49-5
1-FLUORO-3-METHOXYBENZENE
m-Fluoroanisole
Benzene, 1-fluoro-3-methoxy-
1-fluoro-3-methoxy-benzene
MFCD00000335
Anisole, m-fluoro-
DNQ5WQ6YZK
EINECS 207-267-4
DTXSID90196567
NSC 88277
NSC-88277
3-fluoroanisol
3-fluoro-anisole
3-Fluoro anisole
UNII-DNQ5WQ6YZK
META-FLUOROANISOLE
3-Fluoroanisole, 99%
NCIOpen2_001323
1-Fluoro-3-methoxybenzene #
SCHEMBL166269
SCHEMBL12015252
DTXCID30119058
NSC88277
AKOS000120006
CS-W013500
PS-9185
DB-028503
DB-230849
F0254
NS00044069
EN300-16123
Q63409645
F0001-1238
207-267-4