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m-Fluorotoluene

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Identification
Molecular formula
C7H7F
CAS number
352-70-5
IUPAC name
1-fluoro-3-methyl-benzene
State
State

At room temperature, m-Fluorotoluene is in a liquid state. It is often utilized in organic synthesis and industrial applications.

Melting point (Celsius)
-57.00
Melting point (Kelvin)
216.15
Boiling point (Celsius)
110.00
Boiling point (Kelvin)
383.15
General information
Molecular weight
110.13g/mol
Molar mass
110.1300g/mol
Density
0.9657g/cm3
Appearence

m-Fluorotoluene appears as a colorless liquid with a somewhat sweet aromatic odor. It is clear and typically free of any suspended particles, providing a transparent appearance.

Comment on solubility

Solubility of 1-Fluoro-3-methyl-benzene

1-Fluoro-3-methyl-benzene, also known as m-fluorotoluene, is a chemical compound with interesting solubility characteristics. Its solubility can be influenced by several factors:

  • Polarity: The presence of the fluorine atom introduces some polarity into the molecule, which can affect its interactions with solvents.
  • Solvent Types: 1-Fluoro-3-methyl-benzene is generally more soluble in organic solvents such as:
    • Benzene
    • Toluene
    • Ethanol
  • Water Solubility: This compound shows low solubility in water due to its hydrophobic aromatic structure.

In summary, while 1-fluoro-3-methyl-benzene is compatible with organic solvents, it exhibits limited solubility in polar solvents like water. As noted, "like dissolves like", which means that non-polar solutes generally dissolve better in non-polar solvents.

Interesting facts

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

1-Fluoro-3-methyl-benzene, also known as 3-methylfluorobenzene, is a fascinating compound in the realm of solvents and intermediates in organic synthesis. Here are some engaging insights into this compound:

  • Substituent Effects: The presence of both the fluoro and methyl groups on the benzene ring creates interesting electronic effects, influencing the compound's reactivity and properties. The electron-withdrawing nature of the fluoro group can stabilize certain reaction intermediates, leading to unique pathways in chemical synthesis.
  • Applications: This compound is not merely a laboratory curiosity; it serves as a valuable precursor in the production of various pharmaceuticals and agrochemicals. Its ability to participate in electrophilic aromatic substitution reactions allows chemists to introduce further functional groups onto the aromatic system.
  • Environmental Impact: Fluorinated compounds, including 1-fluoro-3-methyl-benzene, have drawn attention concerning their environmental behavior. While their stability can be advantageous in industrial applications, it also poses challenges regarding biodegradability and potential accumulation in ecosystems.
  • Synthesis: One common method for synthesizing 1-fluoro-3-methyl-benzene is through nucleophilic aromatic substitution reactions. For instance, when starting with 3-methylphenol, the introduction of a fluoride source can efficiently produce the fluoro-substituted product.
  • Thermodynamic Stability: The stability of this compound can be examined through its bond strength and enthalpy changes during reactions, providing deeper insights into the nature of chemical bonding in substituted aromatic systems.

As a student or professional in the field of chemistry, diving into compounds like 1-fluoro-3-methyl-benzene opens up a wealth of knowledge concerning organic synthesis, reactivity patterns, and environmental considerations. Remember, the subtle changes in molecular structure can lead to significant differences in chemical behavior!

Synonyms
3-Fluorotoluene
352-70-5
1-Fluoro-3-methylbenzene
M-FLUOROTOLUENE
Benzene, 1-fluoro-3-methyl-
Toluene, m-fluoro-
1-Fluoro-3-methyl-benzene
1-Methyl-3-fluorobenzene
3-Fluorobenzyl radical
F72W445DQ0
NSC 8860
NSC-8860
EINECS 206-524-8
M-FLUOROTOLUENE [MI]
CHEMBL345698
DTXSID2059855
EC 206-524-8
2599-73-7
3fluorotoluene
mTolyl fluoride
UNII-F72W445DQ0
Toluene, mfluoro
meta-Fluorotoluene
1Fluoro3methylbenzene
1Methyl3fluorobenzene
M-TOLYL FLUORIDE
Benzene, 1fluoro3methyl
3-Fluorotoluene, 99%
Toluene, mfluoro (8CI)
Toluene, m-fluoro-(8CI)
SCHEMBL11881
1-fluoranyl-3-methyl-benzene
DTXCID5038961
NSC8860
DTXSID001031339
BDBM50008564
MFCD00000339
STL301893
AKOS000119943
PS-11961
DB-023924
F0040
NS00005603
EN300-19503
m-Fluorotoluene [UN2388] [Flammable liquid]
A822704
Q27277748
F0001-1021
Z104474044
206-524-8