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2-Iodothiophene

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Identification
Molecular formula
C4H3IS
CAS number
4809-23-4
IUPAC name
2-iodothiophene
State
State

At room temperature, 2-Iodothiophene is typically in a liquid state.

Melting point (Celsius)
-30.00
Melting point (Kelvin)
243.15
Boiling point (Celsius)
206.00
Boiling point (Kelvin)
479.15
General information
Molecular weight
221.00g/mol
Molar mass
221.0060g/mol
Density
1.9730g/cm3
Appearence

2-Iodothiophene is a yellowish liquid. It is characterized by its pale yellow appearance, which is typical for many iodinated aromatic compounds.

Comment on solubility

Solubility of 2-Iodothiophene

2-Iodothiophene is an intriguing compound when it comes to solubility, primarily due to its unique structure that combines both a heterocyclic ring and a halogen substituent. Here are some key points regarding its solubility:

  • Solvent Compatibility: 2-Iodothiophene is generally more soluble in organic solvents such as ethanol, acetone, and methanol compared to water. This is indicative of its relatively nonpolar characteristics.
  • Hydrophobic Character: The presence of the sulfur atom and the iodine substituent contributes to a hydrophobic nature, making it less likely to dissolve in polar solvents like water.
  • Temperature Dependency: As with many organic compounds, solubility can increase with temperature. Warmer conditions may enhance the solubility of 2-iodothiophene in organic solvents, allowing for better interaction with the solvent molecules.
  • Functional Group Influence: The presence of the thiophene ring adds interesting properties to the solubility profile, as these types of compounds can engage in various intermolecular forces, sometimes resulting in unique solubility patterns.

In summary, while 2-iodothiophene does not exhibit high solubility in water, it shows promising solubility in a range of organic solvents, making it versatile for various chemical applications. Understanding the solubility of this compound is crucial for those looking to utilize it in different experimental setups.

Interesting facts

Interesting Facts About 2-Iodothiophene

2-Iodothiophene is a fascinating compound that plays a notable role in organic synthesis and materials science. Here are some intriguing aspects of this compound:

  • Structure: 2-Iodothiophene consists of a thiophene ring, which is a five-membered aromatic ring containing sulfur. The presence of iodine in the 2-position adds distinct properties that can be exploited in various chemical reactions.
  • Reactivity: The iodide substituent makes 2-iodothiophene a valuable building block for the synthesis of more complex organic molecules. It can participate in reactions such as nucleophilic substitutions and cross-coupling reactions, making it a versatile compound in synthetic organic chemistry.
  • Applications: This compound finds utility in the fields of material science and pharmaceutical research. It has been utilized in the development of electronic materials, organic solar cells, and various biologically active compounds.
  • Chemical Significance: 2-Iodothiophene serves as an important intermediate in the synthesis of thiophene-containing polymers and other derivatives, enhancing its relevance in advanced materials.
  • Research Interest: Scientists continue to explore the potential of compounds like 2-iodothiophene in developing new methods for functionalizing thiophene rings, paving the way for innovative applications in organic electronics and nanotechnology.

In summary, 2-iodothiophene is more than just a simple organic compound; its unique characteristics and reactivity open doors to numerous research opportunities and applications. As chemistry continues to evolve, the potential for 2-iodothiophene and its derivatives will likely expand, further solidifying its importance in the realm of chemical innovation.

Synonyms
2-IODOTHIOPHENE
Thiophene, 2-iodo-
NSC 1082
EINECS 222-342-1
DTXSID0063026
DTXCID0038835
222-342-1
inchi=1/c4h3is/c5-4-2-1-3-6-4/h1-3
roimnswdojcbfr-uhfffaoysa-n
3437-95-4
2-Thienyl iodide
2-iodo-thiophene
alpha-Iodothiophene
.alpha.-Iodothiophene
MFCD00005424
Iodothiophene
149762-92-5
Z4KJ38KVA6
NSC-1082
Thiophene, iodo-
2-iodo thiophene
NSC1082
2-Iodothiophene over Cu
2-Iodothiophene, 98%
UNII-Z4KJ38KVA6
BIDD:GT0507
SCHEMBL155532
STR02125
AKOS015853948
AC-4904
CS-W007589
SY001504
DB-001036
DB-021243
I0374
NS00029649
EN300-87368
A15989
F0001-1002