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m-Anisole

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Identification
Molecular formula
C7H7ClO
CAS number
2847-92-9
IUPAC name
1-chloro-3-methoxy-benzene
State
State

State at room temperature: It is a liquid.

Melting point (Celsius)
5.20
Melting point (Kelvin)
278.35
Boiling point (Celsius)
210.50
Boiling point (Kelvin)
483.65
General information
Molecular weight
142.58g/mol
Molar mass
142.5780g/mol
Density
1.0869g/cm3
Appearence

Appearance: 1-Chloro-3-methoxybenzene is a colorless to pale yellow liquid.

Comment on solubility

Solubility of 1-chloro-3-methoxy-benzene

1-chloro-3-methoxy-benzene, known for its distinct molecular structure, exhibits varied solubility properties that are essential for its application in different chemical processes. When discussing the solubility of this compound, consider the following aspects:

  • Polarity: The presence of the chloro and methoxy groups introduces a moderate polarity to the molecule. However, the aromatic ring tends to dominate the overall characteristics.
  • Solvent Compatibility: 1-chloro-3-methoxy-benzene is generally more soluble in non-polar solvents like ether and benzene versus polar solvents like water. This behavior can be attributed to its hydrophobic aromatic character.
  • Temperature Influence: Solubility can also vary with temperature; increasing temperature often enhances solubility in organic solvents due to the increased kinetic energy of molecules.

In summary, “solubility is a complex interplay of molecular structure and solvent characteristics.” 1-chloro-3-methoxy-benzene showcases the importance of understanding these factors, as it is primarily soluble in organic solvents while demonstrating minimal solubility in water. This understanding is vital for chemists when considering reaction conditions and extraction methods.

Interesting facts

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

1-Chloro-3-methoxy-benzene, also known as 3-chloroanisole, is an intriguing organic compound that belongs to the family of chlorinated aromatic compounds. This compound has a variety of applications and fascinating characteristics worth noting:

  • Historical Significance: The discovery of chlorinated aromatic compounds like 1-chloro-3-methoxy-benzene paved the way for various modern chemical syntheses and applications in different fields.
  • Flavor and Fragrance: This compound is often used in the synthesis of fragrances and flavoring agents, giving it a notable presence in the food and cosmetic industries.
  • Biological Activity: Some studies have indicated that 1-chloro-3-methoxy-benzene exhibits antibacterial properties, making it of interest for potential medicinal uses.
  • Environmental Concerns: Being a chlorinated compound, it is crucial to monitor the environmental impact of 1-chloro-3-methoxy-benzene, as chlorinated aromatic compounds have been associated with various ecological issues.
  • Molecular Versatility: The presence of both a methoxy group and a chlorine atom provides a platform for further chemical modifications, allowing researchers to create derivatives with novel properties.

In summary, 1-chloro-3-methoxy-benzene exemplifies the balance between utility and concerns in chemical practice. As highlighted by chemist Robert H. Grubbs, "The richness of organic synthesis lies in its ability to generate a vast diversity of compounds that can lead to new discoveries." This compound certainly embodies that richness.

Synonyms
3-Chloroanisole
1-CHLORO-3-METHOXYBENZENE
m-Chloroanisole
Benzene, 1-chloro-3-methoxy-
Anisole, m-chloro-
meta-Chloroanisole
EINECS 220-642-7
m-Chlorophenyl methyl ether
DTXSID7062667
DTXCID9037820
220-642-7
inchi=1/c7h7clo/c1-9-7-4-2-3-6(8)5-7/h2-5h,1h
yukiltjwfrtxgb-uhfffaoysa-n
2845-89-8
3-Chloromethoxybenzene
MFCD00000591
1-chloro-3-methoxy-benzene
3-chloroanisol
3-anisolyl chloride
m-Chloromethoxybenzene
3-methoxychlorobenzene
m-methoxyphenyl chloride
3-methoxyphenyl chloride
3-Chloroanisole, 98%
4-Chloro-2-methoxybenzene
HQ8W659XSK
SCHEMBL70822
SCHEMBL12015248
BCP24449
AKOS008947783
CS-W018269
GS-3089
SY009231
NS00028488
EN300-16118
F13566
3-Chloroanisole, Vetec(TM) reagent grade, 98%
2,1,3-Benzothiadiazole-4-propanoicacid,a-[[(2-hydroxyphenyl)methylene]amino]-