Ammonium, 2-(dimethylamino)-1,3-dithiolanium, bromide
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- Molecular formula
- C5H12BrNS2
- CAS Number
- 7215-34-5
- IUPAC Name
- 1,3-dithiolan-2-ylidene(dimethyl)ammonium;bromide
- Molecular Weight
- 348.33g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.6700g/cm3
- Synonyms
- (1, 3-Dithiolan-2-ylidene)dimethylammonium bromide
Identification
Interesting facts
Interesting Facts about 1,3-Dithiolan-2-ylidene(dimethyl)ammonium Bromide
1,3-Dithiolan-2-ylidene(dimethyl)ammonium bromide is a fascinating compound that showcases the chemistry of sulfur and its unique interactions. Here are some intriguing points to consider:
- Unique Structure: This compound contains a dithiolane ring, which is a five-membered ring that introduces significant strain and intriguing reactivity patterns in synthetic chemistry.
- Ylidene Character: The presence of a ylidene functional group is particularly notable. Ylidenes are known for their reactivity and ability to participate in various chemical reactions, especially in organic synthesis.
- Applications: Compounds such as this one potentially serve as intermediates in the production of more complex organic molecules. They could be useful in pharmaceutical chemistry where sulfur-containing compounds often exhibit biological activity.
- Salt Formation: The bromide ion in this compound acts as a counterion, stabilizing the ammonium cation. Salts of this nature are often used in ionic liquids or as electrolytes in various applications.
- Reactivity: The sulfur atoms in the dithiolane ring can lead to interesting nucleophilic and electrophilic behavior, making the compound a versatile reagent in synthetic methods.
As a chemical scientist, you might find it fascinating how the interplay of sulfur chemistry and ammonium functionalities can lead to innovative applications, particularly in creating complex molecules for pharmaceuticals and agrochemicals. The potential for this compound in organic synthesis highlights the importance of understanding both its structure and its reactivity in advancing chemical science.