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ortho-Tolylchlorocumene

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Identification
Molecular formula
C10H13Cl
CAS number
36507-48-1
IUPAC name
2-chloro-4-isopropyl-1-methyl-benzene
State
State

2-chloro-4-isopropyl-1-methyl-benzene is typically a liquid at room temperature.

Melting point (Celsius)
-43.00
Melting point (Kelvin)
230.15
Boiling point (Celsius)
216.00
Boiling point (Kelvin)
489.15
General information
Molecular weight
168.66g/mol
Molar mass
168.6610g/mol
Density
0.9722g/cm3
Appearence

2-chloro-4-isopropyl-1-methyl-benzene is a colorless liquid.

Comment on solubility

Solubility of 2-chloro-4-isopropyl-1-methyl-benzene

The solubility of 2-chloro-4-isopropyl-1-methyl-benzene, also known as p-chloro-α-methylstyrene, is influenced by its molecular structure and properties. As a substituted aromatic compound, it tends to have limited solubility in water due to the following reasons:

  • Hydrophobic Character: The benzene ring and isopropyl groups contribute to a hydrophobic environment, making it less likely to interact with polar solvents like water.
  • Polarity of the Chlorine Atom: The presence of the chlorine atom adds some polarity, but this is not enough to overcome the hydrophobic effects of the aromatic system.
  • Intermolecular Forces: London dispersion forces dominate in non-polar solvents, while dipole-dipole interactions may play a role in its slight solubility in solvents such as ethanol or acetone.

In summary, while 2-chloro-4-isopropyl-1-methyl-benzene is expected to be poorly soluble in water, it can find moderate solubility in organic solvents. Its interactions are primarily characterized by hydrophobic effects and limited polarity, creating distinct solubility behaviors.

Interesting facts

Interesting Facts About 2-Chloro-4-Isopropyl-1-Methylbenzene

2-Chloro-4-isopropyl-1-methylbenzene, also known as p-chloro-α-isopropyl-toluene, is a fascinating compound in the world of organic chemistry due to its unique structure and properties. Here are some engaging insights:

  • Functional Groups: This compound contains both a chlorine atom and an isopropyl group attached to the benzene ring, showcasing the diversity of substitution patterns that can exist in aromatic compounds.
  • Industrial Significance: 2-Chloro-4-isopropyl-1-methylbenzene is utilized in the production of various agrochemical products. Its chlorinated form can enhance the effectiveness of certain pesticides.
  • Synthetic Routes: There are several methods for synthesizing this compound, including chlorination of toluene derivatives. Understanding these synthetic pathways is critical for organic chemists.
  • Reactivity: The presence of the chlorine atom in this compound makes it susceptible to nucleophilic substitution reactions. This property can be exploited for producing further derivatives and chemical modifications.
  • Research Applications: Scientists are investigating this compound for its potential in developing new materials and pharmaceuticals, owing to the interesting properties imparted by the chlorinated and branched alkyl substituents.

As one scientist noted, "The beauty of chemistry lies in the unexpected combinations of elements and their transformative reactions!" This sentiment captures the essence of studying compounds like 2-chloro-4-isopropyl-1-methylbenzene, which exemplify the complex interplay between structure and function in organic chemistry. Understanding such compounds not only broadens our knowledge of chemical behavior but also enhances our ability to innovate in fields like materials science and agrochemistry.

Synonyms
p-Cymene, 2-chloro-
Septol
4395-79-3
2-Chlorocymol
2-Chloro-4-isopropyltoluene
Benzene, 2-chloro-1-methyl-4-(1-methylethyl)-
Carvacryl chloride
54411-19-7
2-Chloro-4-isopropyl-1-methylbenzene
Benzene, chloro-1-methyl-4-(1-methylethyl)-
NSC-409886
2-Chloro-1-methyl-4-(propan-2-yl)benzene
Chloro-1-methyl-4-(1-methylethyl)benzene
2-chloro-1-methyl-4-propan-2-ylbenzene
2-Chlorcymol
AI3-07028
RR8EN2PD3Y
SCHEMBL824128
TQP1211
JVIGKRUGGYKFSL-UHFFFAOYSA-N
DTXSID101032192
NSC409886
2-chloro-4-isopropyl-1-methyl-benzene
NSC 409886
2-Chloro-4-isopropyl-1-methylbenzene #
2-Chloro-1-methyl-4-(1-methylethyl)benzene