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Trimethylsilyl N,N-diethylcarbamodithioate

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Identification
Molecular formula
C8H19NS2Si
CAS number
3365-61-1
IUPAC name
trimethylsilyl N,N-diethylcarbamodithioate
State
State

At room temperature, Trimethylsilyl N,N-diethylcarbamodithioate exists as a liquid. Its relatively low melting point indicates that it remains in the liquid state under standard ambient conditions.

Melting point (Celsius)
-49.00
Melting point (Kelvin)
224.15
Boiling point (Celsius)
95.00
Boiling point (Kelvin)
368.15
General information
Molecular weight
221.46g/mol
Molar mass
221.4600g/mol
Density
0.9950g/cm3
Appearence

Trimethylsilyl N,N-diethylcarbamodithioate is a colorless to pale yellow liquid. It may appear slightly oily and is generally clear, with no visible impurities.

Comment on solubility

Solubility of Trimethylsilyl N,N-Diethylcarbamodithioate

Trimethylsilyl N,N-diethylcarbamodithioate, often abbreviated as TMS-C, exhibits some intriguing properties when it comes to solubility. The solubility of this compound can be influenced by various factors, such as:

  • Polarity: The presence of the trimethylsilyl group can enhance solubility in organic solvents due to its non-polar nature, while the carbamodithioate part may contribute to polarity.
  • Solvent Type: TMS-C tends to be more soluble in organic solvents like acetone and ethanol rather than in polar solvents like water.
  • Temperature: Increased temperatures can improve solubility, as solubility typically increases with temperature for most organic compounds.

It is commonly observed that “like dissolves like,” which means that this compound's solubility will be higher in similar non-polar or weakly polar solvents. Moreover, while aqueous solubility is limited, the potential for various applications in organic synthesis makes this compound noteworthy despite its moderate solubility characteristics.

In summary, when working with trimethylsilyl N,N-diethylcarbamodithioate, focusing on the right solvent choice and considering temperature variations will be key to optimizing its solubility in practical applications.

Interesting facts

Interesting Facts about Trimethylsilyl N,N-Diethylcarbamodithioate

Trimethylsilyl N,N-diethylcarbamodithioate is a fascinating compound with a diverse range of applications in both industrial and research settings. Here are some compelling points to consider:

  • Versatile Reactivity: This compound is known for its ability to act as a nucleophilic reagent, making it valuable in various organic synthesis reactions.
  • Functional Group Manipulation: The presence of the carbamodithioate functional group allows for the manipulation and formation of other important chemical compounds, facilitating more complex syntheses.
  • Role in Environmental Chemistry: Due to its unique structure, it can be studied to understand the behavior of organosilicon compounds in the environment, contributing to our knowledge of pollutants and their degradation pathways.
  • Applications in Agriculture: Compounds similar to trimethylsilyl N,N-diethylcarbamodithioate have shown potential as agricultural fungicides, indicating its possible usefulness in improving crop protection.
  • Silicon-Based Chemistry: This compound exemplifies the interplay between silicon chemistry and organic compounds, enriching the area of silicones and their derivatives.

As a scientist or chemistry student, recognizing the potential of such compounds can lead to innovative research and applications. The study of trimethylsilyl N,N-diethylcarbamodithioate is just one example of how intricate and impactful organic and organosilicon chemistry can be.

In summary, the ability to explore its reactivity, environmental impact, and industrial uses makes trimethylsilyl N,N-diethylcarbamodithioate a noteworthy topic in the realm of chemical compounds!

Synonyms
CARBAMIC ACID, DIETHYLDITHIO-, TRIMETHYLSILYL ESTER
18881-57-7
BRN 1934246
Diethyldithione, TMS derivative
DTXSID60172252
DTXCID9094743
OVGUMLRVVXSFAI-UHFFFAOYSA-N
Diethyldithiocarbamic acid trimethylsilyl ester
trimethylsilyl N,N-diethylcarbamodithioate
Carbamodithioic acid, diethyl-, trimethylsilyl ester
trimethylsilyldiethyldithiocarbamate