Skip to main content

3,4-Dibromothiophene

ADVERTISEMENT
Identification
Molecular formula
C4H2Br2S
CAS number
3141-27-7
IUPAC name
3,4-dibromothiophene
State
State

At room temperature, 3,4-Dibromothiophene is typically found as a liquid.

Melting point (Celsius)
19.00
Melting point (Kelvin)
292.15
Boiling point (Celsius)
238.00
Boiling point (Kelvin)
511.15
General information
Molecular weight
269.92g/mol
Molar mass
269.9180g/mol
Density
2.0358g/cm3
Appearence

3,4-Dibromothiophene is a liquid compound with a light yellow color, possibly appearing pale brown. It can be described as a viscous liquid.

Comment on solubility

Solubility of 3,4-Dibromothiophene

3,4-Dibromothiophene, with the chemical formula C4H2Br2S, exhibits interesting solubility characteristics that are pivotal for its applications in organic synthesis and materials science.

Typically, the solubility of 3,4-dibromothiophene can be influenced by several factors:

  • Polarity: As a halogenated compound, it displays moderate polarity due to the presence of bromine atoms, affecting its solubility in various solvents.
  • Solvent Compatibility: This compound is generally soluble in organic solvents such as:
    • Chloroform
    • Toluene
    • Acetone
  • Temperature Sensitivity: Higher temperatures can enhance its solubility in organic media, which is a common trend for many organic compounds.

However, it is relatively insoluble in polar solvents like water due to its hydrophobic character. This characteristic can be summarized by the phrase:

"Like dissolves like."

In conclusion, the solubility of 3,4-dibromothiophene makes it a versatile compound for various chemical applications, highlighting the importance of solvent choice when working with this intriguing compound.

Interesting facts

Interesting Facts About 3,4-Dibromothiophene

3,4-dibromothiophene is a fascinating compound that belongs to the family of thiophenes, which are sulfur-containing heterocycles. This compound is of particular interest due to its unique structure and chemical properties, which allow it to play several roles in various fields, including:

  • Drug Development: The presence of bromine atoms enhances the compound's biological activity, making it a valuable candidate for medicinal chemistry.
  • Material Science: 3,4-dibromothiophene can be utilized in the development of organic semiconductors, which are important for electronic devices.
  • Organic Synthesis: Its reactivity allows it to serve as an intermediate in the synthesis of more complex molecules.

One notable feature of 3,4-dibromothiophene is its planar structure, which contributes to its ability to form π-stacking interactions. This characteristic can significantly influence the electronic properties of materials when used in thin films for applications such as organic photovoltaics.

Additionally, the compound has been studied for its potential photophysical properties. Research has shown that thiophene derivatives can exhibit strong fluorescence, making them appealing for use in sensors and light-emitting devices.

In conclusion, the combination of its unique structural attributes and functional versatility makes 3,4-dibromothiophene an essential compound for researchers in both academic and industrial settings.

Synonyms
3,4-DIBROMOTHIOPHENE
3141-26-2
EINECS 221-546-8
NSC 99007
DTXSID50185336
Thiophene, 3,4dibromo (8CI)
DTXCID60107827
Thiophene, 3,4-dibromo-(8CI)
Thiophene, 3,4dibromo (8CI)(9CI)
Thiophene, 3,4-dibromo-(8CI)(9CI)
221-546-8
Thiophene, 3,4-dibromo-
3,4-dibromo-thiophene
MFCD00005465
NSC99007
3,4-Dibromothiphene
Thiophene,4-dibromo-
3, 4-dibromothiophene
3,4-bis(bromanyl)thiophene
3,4-Dibromothiophene, 99%
BIDD:GT0493
SCHEMBL332154
BCP07494
CS-B0012
STR06268
GEO-00977
NSC-99007
AKOS000282034
AB00432
AC-4900
PS-7568
HY-20022
SY001342
DB-028249
D1676
NS00029087
EN300-85066
A820841
InChI=1/C4H2Br2S/c5-3-1-7-2-4(3)6/h1-2