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2,4-Dimethylthiophene

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Identification
Molecular formula
C6H8S
CAS number
15679-12-6
IUPAC name
2,4-dimethylthiophene
State
State

At room temperature, 2,4-Dimethylthiophene is in a liquid state.

Melting point (Celsius)
-48.00
Melting point (Kelvin)
225.20
Boiling point (Celsius)
136.10
Boiling point (Kelvin)
409.30
General information
Molecular weight
112.20g/mol
Molar mass
112.2010g/mol
Density
0.9403g/cm3
Appearence

2,4-Dimethylthiophene is a clear, colorless liquid with a distinctive sulfuric odor. It is a derivative of thiophene, characterized by two methyl groups substituting hydrogen atoms on the thiophene ring.

Comment on solubility

Solubility of 2,4-Dimethylthiophene

2,4-Dimethylthiophene is an organic compound characterized by its aromatic ring structure, which significantly influences its solubility properties. Generally, thiophenes, including 2,4-dimethylthiophene, exhibit varying solubility in solvents due to their unique molecular features.

Solubility Characteristics:

  • Polarity: 2,4-dimethylthiophene is considered to be relatively non-polar, which affects its solubility in different solvents.
  • Solvent Compatibility: It tends to be soluble in organic solvents such as hexane, benzene, and ethyl acetate, but poorly soluble in water due to its non-polar nature.
  • Temperature Dependency: Solubility might increase with temperature, which is a common trait for many organic compounds.

In conclusion, while 2,4-dimethylthiophene is soluble in a range of organic solvents, its solubility in polar solvents is limited, underscoring the importance of selecting the right solvent for applications involving this compound. As with many organic compounds, understanding the solvent interactions can lead to better utilization in chemical processes and reactions.

Interesting facts

Overview of 2,4-Dimethylthiophene

2,4-Dimethylthiophene is a fascinating organosulfur compound that belongs to the family of thiophenes, which are five-membered aromatic compounds containing a sulfur atom. This compound has garnered attention not only for its unique structure but also for its potential applications in various fields.

Structural Features

The structure of 2,4-dimethylthiophene features a thiophene ring substituted with two methyl groups on the 2nd and 4th positions. This arrangement contributes to the compound's aromatic properties, enhancing its stability and reactivity. Notably, the placement of the methyl groups plays a significant role in its chemical behavior:

  • Electron-donating effect: The methyl groups help stabilize the ring, making it more reactive in electrophilic substitution reactions.
  • Steric hindrance: The spatial arrangement of the methyl substituents influences the compound’s interaction with other chemical species.

Applications and Importance

Research has indicated several interesting applications of 2,4-dimethylthiophene:

  • Organic electronics: It is being explored as a material in organic semiconductors due to its electronic properties.
  • Flavor and fragrance industry: Thanks to its distinctive aromatic characteristics, it can be used as a fragrance component.
  • Synthetic pathway: It serves as a valuable intermediate in the synthesis of complex organic molecules.

Interesting Tidbits

Some intriguing aspects of 2,4-dimethylthiophene include:

  • It can exhibit a range of reactivity depending on the conditions, making it a versatile participant in chemical reactions.
  • This compound illustrates how small structural changes can significantly impact the properties and reactivity of organic compounds.
  • Researchers continue to investigate its behavior under different environmental conditions, which could shed light on its stability and applications.

Overall, 2,4-dimethylthiophene is a notable compound in the field of organic chemistry, representing the intricate balance between structure and reactivity in chemical compounds. Its ongoing study may lead to the discovery of innovative applications in technology and industry.

Synonyms
2,4-Dimethylthiophene
638-00-6
Thiophene, 2,4-dimethyl-
2,4-dimethyl-thiophene
Q9B2TF3UVC
EINECS 211-312-3
UNII-Q9B2TF3UVC
DTXSID40213238
RefChem:82557
DTXCID40135729
211-312-3
CPULIKNSOUFMPL-UHFFFAOYSA-N
MFCD00130082
SCHEMBL40746
SCHEMBL126931
SCHEMBL128534
SCHEMBL131474
SCHEMBL133055
GEO-01226
AKOS005255556
FD03141
AS-50030
SY060377
DB-054551
CS-0152847
NS00042108
EN300-111893
O10605
F013555