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2-tert-butylthiophene

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Identification
Molecular formula
C8H12S
CAS number
19097-13-7
IUPAC name
2-tert-butylthiophene
State
State

At room temperature, 2-tert-butylthiophene is in a liquid state. It is volatile and has a lower density than water.

Melting point (Celsius)
-60.00
Melting point (Kelvin)
213.15
Boiling point (Celsius)
178.00
Boiling point (Kelvin)
451.15
General information
Molecular weight
140.25g/mol
Molar mass
140.2510g/mol
Density
0.9147g/cm3
Appearence

2-tert-butylthiophene is typically a clear and colorless to pale yellow liquid. It has a distinct aromatic odor typical of thiophenes.

Comment on solubility

Solubility of 2-tert-butylthiophene

2-tert-butylthiophene, with its unique molecular structure, exhibits distinct solubility characteristics that are essential for various chemical applications. Understanding its solubility behavior is vital for its use in organic synthesis and materials science.

Solubility Profile

Key points regarding the solubility of 2-tert-butylthiophene include:

  • Solvent Compatibility: This compound is generally more soluble in organic solvents than in water. It tends to dissolve well in:
    • Non-polar solvents such as hexane and benzene
    • Moderately polar solvents like dichloromethane
  • Water Solubility: Given its hydrophobic character due to the bulky tert-butyl group, 2-tert-butylthiophene has limited solubility in water.
  • Temperature Effects: Increasing temperature can enhance solubility in organic solvents, which is an important consideration during dissolution processes.

Overall, the solubility of 2-tert-butylthiophene is influenced by several factors, including the solvent type and temperature. When handling this compound, it’s crucial to consider these factors to achieve desired concentrations and facilitate reactions effectively.

Interesting facts

Interesting Facts About 2-tert-butylthiophene

2-tert-butylthiophene is a fascinating compound that draws the interest of chemists and material scientists alike. Here are some notable aspects:

  • Structure and Features: This compound belongs to the family of thiophenes, known for their five-membered aromatic ring containing a sulfur atom. The presence of a tert-butyl group at the 2-position enhances its stability and alters its electronic properties.
  • Applications: 2-tert-butylthiophene is notably used in organic synthesis and materials science. It serves as a building block for various functional molecules, contributing significantly to the development of organic electronic devices, such as organic light-emitting diodes (OLEDs) and organic solar cells.
  • Unique Reactivity: The introduction of the tert-butyl group increases steric hindrance, which influences the reactivity of the compound. This feature can be leveraged in chemical reactions to generate diverse derivatives with tailored properties.
  • Research Potential: Due to its interesting electronic structure, 2-tert-butylthiophene is researched for its potential in producing novel materials with enhanced electrical conductivity and light absorption characteristics, making it a candidate for next-generation electronic applications.
  • Environmental Considerations: As the push for more sustainable chemical practices grows, compounds like 2-tert-butylthiophene are being examined for their ecological impact and their role in green chemistry initiatives.

In summary, 2-tert-butylthiophene is more than just a simple aromatic compound. Its unique properties and versatility open up avenues for innovation in numerous scientific fields. As one researcher noted, "Understanding and manipulating such compounds is essential for the future of electronics and materials science."

Synonyms
2-tert-Butylthiophene
1689-78-7
Thiophene, 2-(1,1-dimethylethyl)-
Thiophene, 2-tert-butyl-
UNII-R5YF9YW3CR
R5YF9YW3CR
AI3-15885
DTXSID7073270
DTXCID9035412
swcdojgiocvxfm-uhfffaoysa-n
2-(TERT-BUTYL)THIOPHENE
2-T-BUTYLTHIOPHENE
MFCD00089197
2-Tert-butyl-thiophene
Thiophene, (1,1-dimethylethyl)-
SCHEMBL73299
AC4668
STK023315
AKOS000268955
AS-77914
SY014132
DB-006219
Q27287835