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p-cymene

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Identification
Molecular formula
C9H11Cl
CAS number
768-20-1
IUPAC name
1-chloro-4-isopropyl-benzene
State
State

At room temperature, 1-chloro-4-isopropylbenzene is in a liquid state.

Melting point (Celsius)
-30.00
Melting point (Kelvin)
243.15
Boiling point (Celsius)
198.00
Boiling point (Kelvin)
471.15
General information
Molecular weight
154.24g/mol
Molar mass
154.2360g/mol
Density
0.8570g/cm3
Appearence

1-Chloro-4-isopropylbenzene is a colorless liquid with an aromatic odor. It is relatively volatile and can appear as a clear substrate in its liquid state.

Comment on solubility

Solubility of 1-chloro-4-isopropyl-benzene

1-chloro-4-isopropyl-benzene, also known as para-isopropylchlorobenzene, exhibits distinct solubility characteristics due to its unique structure. Solubility in organic solvents is generally favored:

  • Polar solvents: 1-chloro-4-isopropyl-benzene has limited solubility in polar solvents such as water. This is primarily due to the hydrophobic character of the aromatic ring and the isopropyl group.
  • Non-polar solvents: It is highly soluble in non-polar organic solvents, like hexane or toluene, which can effectively solvate the hydrophobic regions of the molecule.
  • Temperature effects: In many cases, temperature can significantly influence solubility, with increased temperatures often enhancing solubility in organic solvents.

In summary, while 1-chloro-4-isopropyl-benzene is poorly soluble in polar solvents, it shows considerable solubility in non-polar environments. This characteristic is essential for applications in various chemical processes, emphasizing the importance of understanding solubility behaviors in organic chemistry.

Interesting facts

Interesting Facts about 1-Chloro-4-isopropyl-benzene

1-Chloro-4-isopropyl-benzene, commonly known as p-chloroisopropylbenzene, is a fascinating compound that falls under the category of aromatic halides. Its structural uniqueness provides it with several notable characteristics and applications.

Chemical Properties and Reactivity

This compound is characterized by the presence of a chlorine atom and an isopropyl group attached to the benzene ring. The following points highlight its significant properties:

  • Aromatic Stability: The benzene ring contributes to a stable structure, making it less reactive compared to aliphatic compounds.
  • Halogen Substitution: The chlorine atom allows for potential substitution reactions, making it useful in organic synthesis.
  • Isopropyl Group Influence: The presence of the bulky isopropyl group can impact the compound's reactivity and steric effects during chemical reactions.

Applications

1-Chloro-4-isopropyl-benzene finds utility in various fields:

  • Organic Synthesis: It serves as a vital reactant or intermediate in the synthesis of pharmaceuticals and agrochemicals.
  • Material Science: Its derivatives play crucial roles in the production of polymers and specialty chemicals.

Safety Considerations

As with many halogenated compounds, safety is paramount:

  • Handling: It is essential to work with this compound in a well-ventilated area, using appropriate safety equipment.
  • Environmental Impact: Care should be taken, as chlorinated hydrocarbons can pose environmental risks.

In summary, 1-chloro-4-isopropyl-benzene presents a blend of interesting chemical properties and broad applications, particularly in the field of organic chemistry. Its ability to participate in substitution reactions makes it a valuable compound for creating various chemical products.

Synonyms
2621-46-7
4-Chlorocumene
Benzene, 1-chloro-4-(1-methylethyl)-
Cumene, p-chloro-
p-Chlorocumene
6TX7ZP9YWU
1-Chloro-4-isopropylbenzene
EINECS 220-061-9
CUMENE, 4-CHLORO-
DTXSID0062559
1-CHLORO-4-(1-METHYLETHYL)BENZENE (ACI)
DTXCID3037464
1-CHLORO-4-(1-METHYLETHYL)BENZENE
220-061-9
1-chloro-4-(propan-2-yl)benzene
p-Chlorcumol
1-chloro-4-propan-2-ylbenzene
4-Chloroisopropylbenzene
UNII-6TX7ZP9YWU
2-(p-Chlorophenyl)propane
1-chloro-4-isopropyl-benzene
SCHEMBL197810
1-Chloro-4-isopropylbenzene #
CAA62146
AKOS017516312
BS-22157
CS-0211648
NS00028050
EN300-119971
G54935
Z1255372793