Interesting facts
Interesting Facts about 2,3,4,5-Tetrachlorothiophene
2,3,4,5-Tetrachlorothiophene is an intriguing compound within the family of thiophenes, which are known for their unique structural and electronic properties. Below are some captivating aspects of this compound:
- Halogenated Nature: The presence of four chlorine atoms introduces significant reactivity and chemical properties that can differ remarkably from non-halogenated thiophenes. This makes it particularly interesting in the realm of organic synthesis and materials science.
- Role in Organic Electronics: Thiophene derivatives, including 2,3,4,5-tetrachlorothiophene, are often explored for use in organic electronic materials, such as semiconductors and photovoltaic cells. Their ability to conduct electricity while maintaining thermal stability is a subject of extensive research.
- Environmental Impact: Compounds like 2,3,4,5-tetrachlorothiophene can also pose environmental challenges. Their persistence in ecosystems raises questions about their long-term effects on wildlife and human health.
- Synthetic Utility: This compound serves as a valuable intermediate in organic synthesis. Chemists utilize it for constructing more complex molecules, expanding the toolbox available for drug discovery and material development.
- Diverse Applications: Beyond electronics, 2,3,4,5-tetrachlorothiophene finds applications in various fields, such as agrochemicals and specialty chemicals, which showcases its versatility as a building block in the chemical industry.
In summary, 2,3,4,5-tetrachlorothiophene embodies a dynamic intersection of chemistry, technology, and environmental science, making it a fascinating subject of study for both researchers and students interested in the multifaceted world of chemical compounds.
Synonyms
Tetrachlorothiophene
Perchlorothiophene
2,3,4,5-TETRACHLOROTHIOPHENE
Penphene
Caswell No. 834
EINECS 227-866-4
EPA Pesticide Chemical Code 074701
BRN 0118374
CP 30487
DTXSID5042451
UNII-X82R7655J4
AI3-25764
NSC-44615
NSC-61442
X82R7655J4
DTXCID3022451
5-17-01-00305 (Beilstein Handbook Reference)
CP-30487
TETRACHLOROTHIOPHENE, 2,3,4,5-
wzxxzhonlfrkgg-uhfffaoysa-n
6012-97-1
Thiophene, tetrachloro-
Pemphene
IF (Fumigant)
TCTP
Tetrachlorothiofene
Penn salt td-183
Tetrachlorthiofen
ENT 25,764
2,3,4,5-Chlorothiophene
NSC 61442
TD-183
Thiophene, 2,3,4,5-tetrachloro-
IF
NSC 44615
2,3,4,5-tetrachloro-thiophene
MFCD00005422
2,4,5-Chlorothiophene
2,4,5-Tetrachlorothiophene
Thiophene,3,4,5-tetrachloro-
WLN: T5SJ BG CG DG EG
IF (fumigant) (VAN)
Tetrachlorthiofen [Czech]
IF (VAN)
Tetrachlorothiophene, 99%
BIDD:GT0655
SCHEMBL433499
CHEMBL443394
NSC44615
NSC61442
Tox21_301370
AKOS015897466
AC-4916
NCGC00255751-01
AS-81689
SY104160
CAS-6012-97-1
DB-053537
CS-0197311
NS00034302
E83848
Q27293665
Solubility of 2,3,4,5-Tetrachlorothiophene
2,3,4,5-tetrachlorothiophene is a chlorinated derivative of thiophene and its solubility in various solvents can be quite interesting. Understanding its solubility behavior is crucial for applications in organic synthesis and materials science.
Solubility Characteristics
Solvents: The solubility of 2,3,4,5-tetrachlorothiophene can generally be summarized as follows:
Furthermore, the presence of multiple chlorine substituents affects both the mechanical and electronic structure of the molecule, leading to variations in solubility. As a rule of thumb, increased halogenation can lead to lower solubility in water due to increased molecular weight and hydrophobic interactions.
In conclusion, the solubility profile of 2,3,4,5-tetrachlorothiophene is dominated by its chlorinated structure, resulting in greater solubility in non-polar environments and limited solubility in polar solvents, shaping its utility in various chemical applications.