Interesting facts
Interesting Facts about 3,4-Dichlorothiolane 1,1-Dioxide
3,4-Dichlorothiolane 1,1-dioxide is a fascinating compound that showcases the intersection of organic chemistry and practical applications. Here are some intriguing aspects to consider:
- Unique Structure: This compound features a thiolane ring with two chlorine atoms substituting at the 3 and 4 positions. The presence of a sulfur atom in its structure provides unique properties and reactivity, distinguishing it from many other cyclic compounds.
- Oxidation State: The term "1,1-dioxide" in its name refers to the incorporation of two oxygen atoms, highlighting the compound's oxidized state, which plays a crucial role in its reactivity and chemical behavior.
- Application Potential: Compounds similar to 3,4-dichlorothiolane 1,1-dioxide have been explored for their utility in various fields, such as pharmaceuticals and agrochemicals. This opens avenues for research into its potential applications in synthesis and catalysis.
- Chlorine's Role: The presence of chlorine atoms greatly influences the reactivity and properties of the compound, making it an area of interest for chemists studying halogenated compounds, which often exhibit remarkable biological activities.
- Environmental Impact: Understanding compounds like 3,4-dichlorothiolane 1,1-dioxide is vital in assessing environmental safety, as halogenated compounds can have significant effects on ecosystems and human health.
As we delve deeper into the chemistry of 3,4-dichlorothiolane 1,1-dioxide, it becomes evident that it not only adds to the repertoire of organic compounds but also serves as a reminder of the complexities and challenges within the field of chemical science. Its study can lead to unexpected discoveries, echoing the sentiments of renowned chemist Linus Pauling: "The best way to have a good idea is to have lots of ideas."
Synonyms
3,4-Dichlorosulfolane
3001-57-8
3,4-Dichlorothiolane 1,1-dioxide
Thiophene, 3,4-dichlorotetrahydro-, 1,1-dioxide
THIOPHENE, TETRAHYDRO-3,4-DICHLORO-, 1,1-DIOXIDE
48DT4BVL3G
3,4-DICHLOROTETRAHYDROTHIOPHENE-1,1-DIOXIDE
NSC-13391
NSC-27866
NSC-35959
jcuqwsialjciee-uhfffaoysa-n
3,4-Dichlorotetrahydrothiophene 1,1-dioxide
DAC PRD
DAC PRO
Dichlorothiolane dioxide
PRD experimental nematocide
NSC 13391
NSC 27866
NSC 35959
20688-41-9
3,4-dichloro-1??-thiolane-1,1-dione
PRD
WLN: T5SWTJ CG DG
Thiophene,4-dichloro-, 1,1-dioxide
Thiophene,4-dichlorotetrahydro-, 1,1-dioxide
UNII-48DT4BVL3G
SCHEMBL435717
DTXSID401031193
DAA00157
NSC13391
NSC27866
NSC35959
BBL011034
MFCD00022537
NSC141368
STK802189
AKOS001046105
AKOS016879873
NSC-141368
VS-02814
3,4-dichloro-1lambda6-thiolane-1,1-dione
DB-047688
EU-0046741
EN300-66913
rac-(3S,4S)-3,4-dichlorothiolane 1,1-dioxide
AE-848/31939004
Z56872217
Thiophene,3,4-dichlorotetrahydro-,1,1-dioxide,(3R,4R)-rel-
Solubility of 3,4-Dichlorothiolane 1,1-Dioxide
The solubility of 3,4-dichlorothiolane 1,1-dioxide presents some interesting characteristics that are important to consider in various applications. This compound is known to exhibit the following solubility properties:
Overall, the solubility behavior can be summarized as:
The unique structure of this compound may contribute to varied **interactions with different solvents**, leading to its applications in organic synthesis and pharmaceutical formulations. Understanding these solubility properties is vital for effective utilization in chemical processes.