Interesting facts
Interesting Facts about Thiocarbonyl Dichloride
Thiocarbonyl dichloride, a compelling compound in the realm of chemistry, garners attention not only for its unique structure but also for its diverse applications and intriguing properties. Below are some fascinating insights into this compound:
- Structure and Bonding: Thiocarbonyl dichloride features a carbon atom double-bonded to a sulfur atom, with two chlorine atoms attached. This arrangement imparts distinct properties due to the combined influence of sulfur and chlorine on reactivity.
- Reactivity: Renowned for its high reactivity, thiocarbonyl dichloride can undergo nucleophilic attack, making it an essential reagent in organic synthesis. It often serves as a precursor for various sulfur-containing compounds.
- Applications: This compound plays a significant role in the production of thioketones and other specialized chemicals. Its reactivity allows it to be instrumental in developing herbicides, pesticides, and pharmaceuticals.
- Safety Considerations: Due to its corrosive nature and potential to release toxic gas upon decomposition, handling thiocarbonyl dichloride requires precautionary measures. Always utilize appropriate protective equipment and work in a well-ventilated area.
- Environmental Impact: While thiocarbonyl dichloride has valuable applications, its environmental persistence and potential bioaccumulation raise concerns. Studying its degradation pathways is essential for developing safe usage protocols.
As the field of chemistry evolves, understanding compounds like thiocarbonyl dichloride can lead to significant advancements in technology and environmental safety. Exploring its properties and effects can inspire future innovations and responsible chemical practices.
Synonyms
THIOPHOSGENE
Thiocarbonyl dichloride
Carbonothioic dichloride
Thiocarbonyl chloride
Carbon chlorosulfide
Dichlorothiocarbonyl
Thiocarbonic dichloride
Thiofosgen
Phosgene, thio-
Thiokarbonylchlorid
Thiofosgen [Czech]
Carbonyl chloride, thio-
Carbonic dichloride, thio-
Thiokarbonylchlorid [Czech]
CSCl2
HSDB 861
EINECS 207-341-6
Dichlorothioformaldehyde
UN2474
UNII-067FQP576P
BRN 1633495
067FQP576P
THIOPHOSGENE [HSDB]
4-03-00-00281 (Beilstein Handbook Reference)
DTXSID2060046
CHEBI:29366
UN 2474
THIOFOSGEN (CZECH)
THIOKARBONYLCHLORID (CZECH)
Carbonyl Sulfide Dichloride
Phosgene, thio
Carbonyl chloride, thio
Carbonic dichloride, thio
DTXCID3040485
thiocarbonyl dichloride;thiophosgene
zwzvwgitaaifps-uhfffaoysa-n
463-71-8
Thiophosgene [UN2474] [Poison]
carbonothioyl dichloride
thiophosgen
thio-phosgene
thiophos-gene
thiophosgene I
SCHEMBL17943
chloromethanecarbothioyl chloride
BCP26011
BBL027488
STL372704
AKOS015919086
VS-08549
NS00043605
T1320
Carbonothioic dichloride;Thiocarbonyl dichloride
A827036
Q421064
Solubility of Thiocarbonyl Dichloride
Thiocarbonyl dichloride (C2Cl2S) is a compound that exhibits interesting solubility properties. Its solubility can be influenced by several factors, including temperature and the presence of specific solvents. Here are some key points to consider:
In conclusion, while thiocarbonyl dichloride is largely insoluble in water, its solubility in organic solvents makes it a valuable compound in synthetic chemistry. Always consider the solvent choice for effective dissolution and application of this interesting compound!