Interesting facts
Exploring Bis(methylsulfanyl)methane
Bis(methylsulfanyl)methane is a fascinating organic compound that showcases the intriguing chemistry of sulfur-containing molecules. This compound stands out for a number of reasons:
- Sulfur's Role: The presence of sulfur atoms in this compound contributes not just to its reactivity but also impacts its physical properties, making it a subject of interest in both industrial applications and research.
- Biological Relevance: Compounds containing methylsulfanyl groups are often researched for their potential biological activities, which can include antimicrobial and antioxidant properties. Such influences can be significant in pharmaceutical applications.
- Dual Functionality: With two methylsulfanyl groups attached to a central methane carbon, this compound exhibits both nucleophilic and electrophilic characteristics, making it versatile in various chemical reactions.
- Applications: The structural features of bis(methylsulfanyl)methane make it a valuable intermediate in organic synthesis, particularly in developing fine chemicals and agrochemicals.
- Simplistic yet Complex: Although the name might suggest simplicity, the compound's behavior in different environments can lead to complex interactions, making it a rich area of study for chemical scientists.
As a student or scientist, delving into the chemistry of bis(methylsulfanyl)methane allows for a greater appreciation of sulfur chemistry and its widespread implications. The connection between molecular structure and reactivity prompts exciting discussions and further exploration within the field.
Synonyms
Bis(methylthio)methane
Bis(methylsulfanyl)methane
Methane, bis(methylthio)-
2,4-DITHIAPENTANE
Bis(methylmercapto)methane
Formaldehyde dimethyl mercaptal
Methylenebis(methyl sulfide)
Thioformaldehyde dimethylacetal
CH3SCH2SCH3
2,4-dithiopentane
Bis[methylmercapto]methane
NSC 96010
UNII-128SGX814T
Thioformaldehyde dimethylthioacetal
128SGX814T
EINECS 216-577-9
NSC-96010
Methylenebis[methyl sulfide]
DTXSID0061822
FEMA NO. 3878
LOCDPORVFVOGCR-UHFFFAOYSA-
BIS(METHYLTHIO)METHANE [MI]
BIS-(METHYLTHIO)METHANE [FHFI]
bis-(Methylthio)methane
Bis(methyl mercapto) methane
DTXCID4035203
inchi=1/c3h8s2/c1-4-3-5-2/h3h2,1-2h3
locdporvfvogcr-uhfffaoysa-n
1618-26-4
Dimethylthiomethane
C3H8S2
MFCD00008564
Bis(methylthio)methan
2, 4-Dithiapentane
Bismethylmercaptomethane
Bis(methylthio)-Methane
bis(methylsulanyl)methane
bis-(methylsulfanyl)-methane
Formaldehyde dimethylmercaptal
Bis(methylthio)methane, 99%
SCHEMBL570237
Thioformaldehyde dimethyl acetal
CHEBI:167064
NSC96010
Bis(methylthio)methane, >=99%, FG
AKOS015897414
CS-W013673
LS-12964
B1204
NS00021721
D88765
EN300-215392
A810297
Q2567203
Solubility of bis(methylsulfanyl)methane
Bis(methylsulfanyl)methane, with its distinct structure, presents interesting solubility characteristics in various solvents. Understanding the solubility of this compound is key to its applications in chemical processes. Here are some important points regarding its solubility:
In summary, while bis(methylsulfanyl)methane may not be readily soluble in water, its solubility profile in organic solvents opens up potential for diverse applications within chemical synthesis and formulation.