Interesting facts
Interesting Facts about 2,5-Dimethylthiophene
2,5-Dimethylthiophene is a fascinating compound that belongs to the class of heterocyclic compounds, specifically thiophenes, which are sulfur-containing aromatic rings. Here are some intriguing aspects of this compound:
- Structure and Symmetry: The structure of 2,5-dimethylthiophene exhibits planar symmetry due to the presence of the sulfur atom in the five-membered ring. This symmetry contributes to its unique electronic properties.
- Uses in Organic Synthesis: 2,5-Dimethylthiophene serves as a valuable intermediate in the synthesis of various organic compounds, including pharmaceuticals and agrochemicals. Its reactivity makes it a key player in multiple chemical reactions.
- Role in Polymer Chemistry: This compound is also utilized in the synthesis of conductive polymers. Its conjugated system allows for the creation of materials with enhanced electrical properties, which have potential applications in electronic devices.
- Odor and Flavor: Interestingly, thiophenes are known for their characteristic odors. 2,5-Dimethylthiophene has a distinctive scent that can be described as earthy or sulfurous, making it a subject of interest in the field of fragrance chemistry.
- Biological Activity: Preliminary studies have indicated that compounds containing thiophene rings, including 2,5-dimethylthiophene, may exhibit various biological activities, potentially including antimicrobial and anti-inflammatory effects. This opens up avenues for further research in medicinal chemistry.
In summary, 2,5-dimethylthiophene is not just an ordinary compound; it embodies the intersection of structure, reactivity, and diverse applications. Its intriguing properties make it a subject of ongoing research in both academic and industrial fields.
Synonyms
2,5-DIMETHYLTHIOPHENE
638-02-8
Thiophene, 2,5-dimethyl-
2,5-dimethyl-thiophene
UNII-V6DDX6WB12
V6DDX6WB12
EINECS 211-313-9
NSC-60689
DTXSID2074295
NSC 60689
Thiophene, 2,5dimethyl
DTXCID0044103
211-313-9
gwqooadxmvqeft-uhfffaoysa-n
inchi=1/c6h8s/c1-5-3-4-6(2)7-5/h3-4h,1-2h
un1993
MFCD00005452
NSC60689
2,5 Dimethylthiophene
Thiophene,5-dimethyl-
2,5-dimethyl thiophene
SCHEMBL64283
2 pound not5-Dimethylthiophene
2,5-Dimethylthiophene, >=98%
2,5-Dimethylthiophene, 98.5%
CHEBI:167073
AKOS000121512
AKOS016017809
PS-3263
AC-18077
SY018010
2,5-Dimethylthiophene, analytical standard
DB-054553
CS-0022382
D1591
NS00022605
EN300-21089
F11266
2,5-Dimethylthiophene, purum, >=98.0% (GC)
Q27291590
F0001-1465
Solubility of 2,5-Dimethylthiophene
2,5-Dimethylthiophene is an organic compound characterized by its distinct aromatic properties. When assessing its solubility, several key factors come into play:
The solubility behavior can be succinctly summarized: "The extent of solubility is largely influenced by the nature of the solvent." Consequently, when working with 2,5-dimethylthiophene, choosing the appropriate solvent is crucial for effective dissolution and subsequent reactions.