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2-bromothiophene

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Identification
Molecular formula
C4H3BrS
CAS number
1003-09-4
IUPAC name
2-bromothiophene
State
State

At room temperature, 2-bromothiophene is a liquid, typically clear or with a slight yellow tinge.

Melting point (Celsius)
-3.50
Melting point (Kelvin)
269.65
Boiling point (Celsius)
159.50
Boiling point (Kelvin)
432.65
General information
Molecular weight
163.04g/mol
Molar mass
163.0490g/mol
Density
1.6177g/cm3
Appearence

2-Bromothiophene appears as a colorless to pale yellow liquid. It is often found in its pure form or as part of formulations and can have a slight aromatic odor associated with its thiophene ring structure.

Comment on solubility

Solubility of 2-bromothiophene

Understanding the solubility of 2-bromothiophene can provide valuable insights into its behavior in various environments. This compound, with the chemical formula C4H3BrS, exhibits specific characteristics when it comes to solubility:

  • Solvent Interaction: 2-bromothiophene is generally soluble in organic solvents such as ethanol, acetone, and chloroform.
  • Water Solubility: It has limited solubility in water, which is common for many aromatic and heterocyclic compounds due to their hydrophobic nature.
  • Temperature Dependency: The solubility can change with temperature. Typically, organic compounds have higher solubility at elevated temperatures.

In summary, while 2-bromothiophene shows good solubility in organic solvents, its limited solubility in water is a key factor to consider in applications such as chemical synthesis or pharmaceutical formulations. As always, appropriate solubility investigations should be conducted based on specific application needs.

Interesting facts

Interesting Facts about 2-Bromothiophene

2-Bromothiophene is a fascinating compound in the field of organic chemistry, particularly renowned for its role in synthesizing various materials, including pharmaceuticals and agrochemicals. Here are some key facts about this intriguing compound:

  • General Structure: 2-Bromothiophene consists of a thiophene ring, a five-membered aromatic structure that contains a sulfur atom, making it unique and reactivity-rich.
  • Applications: This compound is widely utilized in the synthesis of functionalized materials, including conducting polymers and dye-sensitized solar cells.
  • Reactivity: 2-Bromothiophene is an excellent substrate for various organic reactions due to the presence of the bromine atom, which acts as a leaving group in nucleophilic substitutions and coupling reactions.
  • Chemical Versatility: The presence of the bromine group allows for further transformations, making it a valuable building block for the creation of more complex molecules involved in drug discovery.
  • Research Interest: Studies show that thiophene derivatives, including 2-bromothiophene, can exhibit interesting optical and electronic properties, which have implications in the development of organic semiconductors.

In the world of synthetic chemistry, 2-bromothiophene stands out not only for its structural elegance but also for its practical applications. As subsequent research and innovation continue to evolve, one can expect to uncover even more potential uses and characteristics of this remarkable compound.

Synonyms
2-BROMOTHIOPHENE
1003-09-4
Thiophene, 2-bromo-
2-Thienyl bromide
GFF929NUW7
NSC 4456
NSC-4456
EINECS 213-699-4
DTXSID4061389
2Thienyl bromide
Thiophene, 2bromo
DTXCID7032509
213-699-4
inchi=1/c4h3brs/c5-4-2-1-3-6-4/h1-3
Thiophene, bromo-
Bromothiophene
2-bromo-thiophene
2-bromo thiophene
MFCD00005417
60326-18-3
Thienyl bromide
5-bromothiophene
NSC4456
5-bromo-thiophene
2-bromanylthiophene
2-Bromothiophene, 98%
UNII-GFF929NUW7
SCHEMBL22395
BIDD:GT0231
BCP21550
AC-194
AKOS000121588
CS-W020109
DS-1962
FB02219
PS-5772
DB-020745
B0941
NS00022968
EN300-20745
D77872
A800095
Q17487944
F0001-0036