Interesting facts
Interesting Facts about 2,5-Dihydrothiophene 1,1-Dioxide
2,5-Dihydrothiophene 1,1-dioxide is a fascinating compound in the realm of organosulfur chemistry. Here are some intriguing insights about this compound:
- Structural Uniqueness: It features a five-membered ring containing sulfur, making it a member of a broader family of thiophenes. This unique structure is responsible for its interesting reactivity and potential applications.
- Functional Group Influence: The dioxide functionality significantly enhances the compound's reactivity, allowing it to participate in various chemical transformations that could be exploited in synthetic organic chemistry.
- Applications: Due to its unique properties, 2,5-dihydrothiophene 1,1-dioxide is studied for its potential use in pharmaceuticals, agrochemicals, and the development of new materials. It can be involved in the formation of heterocyclic compounds which are important in drug design.
- Natural Occurrence: Compounds related to thiophenes are often found in certain natural products, suggesting that they might play a role in biological systems, although the specific biological function of 2,5-dihydrothiophene 1,1-dioxide remains under investigation.
- Research Dynamics: Ongoing research is delving into the synthesis and characterization of 2,5-dihydrothiophene 1,1-dioxide, exploring its potential as an intermediate in various chemical reactions, notably in the synthesis of pharmaceutical compounds.
As a chemistry student or scientist, you may find that studying compounds like 2,5-dihydrothiophene 1,1-dioxide not only enriches your understanding of organosulfur chemistry but also opens new avenues for innovation in various industrial applications. Emphasizing research in this area could lead to significant breakthroughs!
In the words of chemists, "Understanding the underlying chemistry of compounds like 2,5-dihydrothiophene 1,1-dioxide is crucial for the advancement of science and technology."
Synonyms
3-Sulfolene
77-79-2
2,5-DIHYDROTHIOPHENE 1,1-DIOXIDE
Butadiene sulfone
Sulfolene
beta-Sulfolene
Thiophene, 2,5-dihydro-, 1,1-dioxide
2,5-Dihydrothiophene sulfone
2,5-Dihydrothiophene dioxide
sulpholene
2,5-dihydrothiophene-1,1-dioxide
.beta.-Sulfolene
NCI-C04557
CCRIS 569
HSDB 2903
EINECS 201-059-7
1-Thia-3-cyclopentene 1,1-dioxide
NSC 48532
UNII-Z6003L44MN
BRN 0107004
DTXSID6021294
AI3-23457
2,5-dihydrothiophene s,s-dioxide
Butadiene-2,2,5,5-D4 sulfone
NSC-48532
NSC-56373
3-SULFOLENE [MI]
2,5-dihydro-1??-thiophene-1,1-dione
DTXCID801294
2,5-dihydrothiophen-1,1-dioxide
Z6003L44MN
Thiophene, dihydro-, 1,1-dioxide
5-17-01-00177 (Beilstein Handbook Reference)
WLN: T5SW CUTJ
Thiophene,5-dihydro-, 1,1-dioxide
CAS-77-79-2
Sulfol-3-ene
betaSulfolene
MFCD00005481
2,5-Dihydro-1-thiophene-1,1-dione
Boc-Ile-OH.5H2O
2,5-dihydro-1lambda6-thiophene-1,1-dione
Butadiene sulfone, 98%
2,5Dihydrothiophene dioxide
2,5Dihydrothiophene sulfone
SCHEMBL93157
1Thia3cyclopentene 1,1dioxide
2,5Dihydrothiophene 1,1dioxide
CHEMBL3182104
CHEBI:194619
NSC48532
NSC56373
Tox21_201532
Tox21_302817
2,5-Dihydro-thiophene 1,1-dioxide
2,5-Dihydrothiophene, 1,1-dioxide
NSC119477
STK331115
Thiophene, 2,5dihydro, 1,1dioxide
AKOS000119153
FS61272
NSC-119477
NCGC00249061-01
NCGC00256473-01
NCGC00259082-01
AS-60909
DB-045441
DB-056257
D0557
NS00022788
EN300-18108
THIOPHENE, 2-5-DIHYDRO-1.1-DIOXIDE
F74854
Q601018
Z57161872
F1294-0012
Solubility of 2,5-Dihydrothiophene 1,1-Dioxide
2,5-Dihydrothiophene 1,1-dioxide, identified by its chemical formula as C4H6O2S, exhibits notable solubility characteristics that can be highlighted as follows:
In summary, the solubility of 2,5-dihydrothiophene 1,1-dioxide can be summarized as follows: it is soluble in polar solvents but less so in non-polar environments, exhibiting its versatile nature in chemical applications.