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2-Chloro-4-ethylphenol

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Identification
Molecular formula
C8H9ClO
CAS number
94-94-0
IUPAC name
2-chloro-4-ethyl-phenol
State
State

At room temperature, it is in a solid state, often presented as crystals or powder with a phenolic odor.

Melting point (Celsius)
49.00
Melting point (Kelvin)
322.15
Boiling point (Celsius)
276.00
Boiling point (Kelvin)
549.15
General information
Molecular weight
156.61g/mol
Molar mass
156.6130g/mol
Density
1.1630g/cm3
Appearence

2-Chloro-4-ethylphenol typically appears as colorless to pale yellow crystals or solid. It might have a distinct phenolic or sweetish odor.

Comment on solubility

Solubility of 2-chloro-4-ethyl-phenol

2-chloro-4-ethyl-phenol, with the formula C10H13ClO, exhibits interesting solubility characteristics that are vital for its applications in various chemical processes.

Key Points on Solubility

  • Solvent Interaction: This compound is known to be soluble in organic solvents such as ethanol, acetone, and chloroform due to its hydrophobic aromatic structure.
  • Limited Water Solubility: 2-chloro-4-ethyl-phenol displays poor solubility in water, primarily because of the presence of the bulky ethyl group and the chlorine substituent which hinder hydrogen bonding with water molecules.
  • Temperature Dependence: Solubility may vary with temperature; generally, higher temperatures can increase the solubility of organic compounds in solvents.
  • pH Influence: The solubility of 2-chloro-4-ethyl-phenol can also be affected by the pH of the solution, as its acidity or basicity may change under different conditions.

In summary, while 2-chloro-4-ethyl-phenol is soluble in organic solvents, its limited water solubility is an important consideration in both laboratory and industrial settings. Understanding the solubility profile is essential for practical applications, including formulation and processing.

Interesting facts

Interesting Facts about 2-Chloro-4-ethyl-phenol

2-Chloro-4-ethyl-phenol is a fascinating compound that belongs to the family of chlorophenols, which are known for their versatile applications in various fields. Here are some intriguing aspects of this compound:

  • Structure and Isomerism: As a chlorinated phenol, 2-chloro-4-ethyl-phenol exhibits interesting structural isomerism. The position of the chlorinated substituent and the ethyl group can significantly influence its properties and reactivity.
  • Applications: This compound is commonly used as an intermediate in the synthesis of agrochemicals, pharmaceuticals, and various chemical products. Its unique properties make it a potential candidate for research in novel material development.
  • Biological Activity: Interestingly, some chlorophenols are studied for their antimicrobial properties. This invites investigations into the potential health benefits or hazards associated with exposure to compounds like 2-chloro-4-ethyl-phenol.
  • Environmental Considerations: As with many halogenated compounds, studying the environmental impact of 2-chloro-4-ethyl-phenol is crucial. Understanding its persistence in the ecosystem and its degradation pathways can help in managing its use responsibly.
  • Chemical Reactivity: The presence of the chlorine atom in its structure makes this compound highly reactive. It can participate in various chemical reactions, including nucleophilic substitutions, which are vital in organic synthesis.

In summary, 2-chloro-4-ethyl-phenol is not just a simple molecule, but a compound that opens doors to a wide array of scientific inquiries. Its diversity in applications and implications for health and the environment make it a worthy subject of study.

Synonyms
2-Chloro-4-ethylphenol
18980-00-2
PHENOL, 2-CHLORO-4-ETHYL-
BRN 1862344
2-CHLORO-4-ETHYL-PHENOL
4-Chlor-2-aethylphenol [German]
PHENOL,2-CHLORO-4-ETHYL-
MFCD16997710
4-Chlor-2-aethylphenol
Q6AJS79TJ9
SCHEMBL157976
SCHEMBL27719648
SCHEMBL30582486
ALBB-032446
AKOS005288299
MB23911
LS-12033
DB-260904
EN300-843567
H46342
4-06-00-03013 (Beilstein Handbook Reference)