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2,3,4-Trimethylthiophene

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Identification
Molecular formula
C7H10S
CAS number
16400-61-6
IUPAC name
2,3,4-trimethylthiophene
State
State

At room temperature, 2,3,4-trimethylthiophene is in a liquid state, which is typical for lower-molecular-weight thiophenes and similar heterocyclic compounds.

Melting point (Celsius)
-45.00
Melting point (Kelvin)
228.15
Boiling point (Celsius)
163.00
Boiling point (Kelvin)
436.15
General information
Molecular weight
126.23g/mol
Molar mass
126.2290g/mol
Density
0.9222g/cm3
Appearence

2,3,4-Trimethylthiophene is a colorless to light yellow liquid with a faint characteristic odor. Its transparency allows it to be identified easily in various settings and applications.

Comment on solubility

Solubility of 2,3,4-trimethylthiophene

2,3,4-trimethylthiophene, with its unique structure, exhibits varying solubility characteristics that are intriguing for both industrial and research applications. Understanding its solubility can help in predicting how it interacts in different environments. Here are some key points:

  • Solvent Preferences: 2,3,4-trimethylthiophene is generally soluble in organic solvents such as ethanol, acetone, and dichloromethane, which can dissolve many non-polar or weakly polar compounds.
  • Water Solubility: This compound has very low solubility in water due to its non-polar characteristics, which hinder its ability to interact favorably with the polar water molecules.
  • Influencing Factors: Factors such as temperature, pressure, and the presence of other solutes can significantly influence the solubility of 2,3,4-trimethylthiophene in various solvents.

In summary, 2,3,4-trimethylthiophene's solubility behavior responds distinctly to solvent polarity and molecular interactions, making it an interesting study subject in solubility dynamics.

Interesting facts

Interesting Facts about 2,3,4-Trimethylthiophene

2,3,4-Trimethylthiophene is a fascinating compound that belongs to the thiophene family, which is known for its aromatic and heterocyclic characteristics. Here are some intriguing aspects of this compound:

  • Structure and Stability: The compound features a five-membered ring structure containing a sulfur atom, which significantly contributes to its aromatic properties and stability.
  • Origin: 2,3,4-Trimethylthiophene is often found in various natural sources, including certain essential oils, and has been identified as a component of several plant extracts.
  • Scent Profile: This compound is recognized for its distinctive odor, which can be described as sweet and somewhat nutty. Such aromatic qualities make it attractive in flavoring and fragrance industries.
  • Applications: Beyond its sensory qualities, 2,3,4-trimethylthiophene has potential applications in organic synthesis and the development of various functional materials due to its unique structural properties.
  • Aromatic Compounds: Compounds like 2,3,4-trimethylthiophene are vital in understanding the behavior of aromatic compounds and their interactions, which can have implications in fields ranging from materials science to pharmacology.

In sum, 2,3,4-trimethylthiophene is more than just a chemical entity; it represents a rich area of study with implications for both theoretical and applied chemistry. As we continue to explore such compounds, we uncover the interconnectedness of chemical properties, natural products, and industrial applications.

Synonyms
Thiophene, 2,3,4-trimethyl-
2,3,4-TRIMETHYLTHIOPHENE
3NN5DSQ4CT
DTXSID2073277
EINECS 217-268-1
DTXCID2035695
217-268-1
mavvdcdmbkfues-uhfffaoysa-n
1795-04-6
trimethylthiophene
UNII-3NN5DSQ4CT
SCHEMBL765340
AT33158
NS00047865