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S-ethyl chloromethanethioate

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Identification
Molecular formula
C3H7ClS
CAS number
2941-21-1
IUPAC name
S-ethyl chloromethanethioate
State
State

It is a liquid at room temperature, typically clear or with a faint yellowish tint.

Melting point (Celsius)
-92.50
Melting point (Kelvin)
180.65
Boiling point (Celsius)
64.80
Boiling point (Kelvin)
337.95
General information
Molecular weight
126.62g/mol
Molar mass
126.6210g/mol
Density
1.1361g/cm3
Appearence

S-ethyl chloromethanethioate is a clear to pale yellow liquid with a discernible, pungent odor. As a liquid, it can be observed to have a smooth flow and is often stored in opaque containers to protect it from light.

Comment on solubility

Solubility of S-ethyl chloromethanethioate

S-ethyl chloromethanethioate, with its distinctive chemical structure, exhibits intriguing properties related to solubility. Understanding its solubility can provide insight into its potential applications and behavior in various environments. Here are some key points to consider:

  • Polarity: The presence of the chloromethyl group contributes to a degree of polarity in the molecule, which influences its solubility in polar solvents.
  • Solvent Compatibility: Generally, S-ethyl chloromethanethioate is expected to be soluble in organic solvents such as ethyl acetate and acetone, while exhibiting limited solubility in water due to its hydrophobic characteristics.
  • Impact of Temperature: Like many organic compounds, solubility may increase with temperature, making heated solvents more effective for dissolving S-ethyl chloromethanethioate.
  • Applications: The solubility profiles are essential for applications in chemical synthesis and in formulating pesticides, where the effective delivery of the compound is crucial.

As a general rule, the solubility of S-ethyl chloromethanethioate can be summarized as follows: compatible with non-polar to slightly polar solvents while being less favorable in polar solvents such as water. This leads to its successful utilization in various chemical processes.

Thus, understanding the solubility characteristics of this compound not only aids in its application but also in predicting its environmental behavior and interactions.

Interesting facts

Interesting Facts about S-ethyl chloromethanethioate

S-ethyl chloromethanethioate is a fascinating compound with applications that highlight the versatility of organosulfur chemistry. This compound is particularly noted for its role in the synthesis of various agrochemicals and pharmaceuticals. Here are some key points to consider:

  • Organosulfur Compounds: S-ethyl chloromethanethioate belongs to a class of compounds known as organosulfur compounds, which are characterized by the presence of sulfur atoms in their molecular structure. These compounds often display unique properties and reactivities that can be harnessed in chemical synthesis.
  • Role in Synthesis: This compound serves as an important intermediate in the formation of other chemicals. Its functionality allows chemists to introduce thioether or thioester groups into more complex organic molecules.
  • Impact on Agriculture: As a precursor to various agrochemicals, S-ethyl chloromethanethioate is utilized in the development of herbicides and pesticides, playing a pivotal role in modern agricultural practices aimed at improving crop yields.
  • Safety Precautions: It is essential to handle this compound with care due to its potential reactivity. Proper laboratory protocols and personal protective equipment are strongly recommended when working with S-ethyl chloromethanethioate to ensure safe handling.
  • Research Potential: The ongoing research into organosulfur compounds like S-ethyl chloromethanethioate expands our understanding of their chemical properties and potential applications in various fields, including medicinal chemistry and environmental science.

In summary, S-ethyl chloromethanethioate is more than just a chemical entity; it embodies the intersection of chemistry, agriculture, and innovation. Its role as a valuable building block in synthetic chemistry demonstrates the importance of this compound in various industrial applications.

As the renowned chemist Linus Pauling once said, "The best way to have a good idea is to have a lot of ideas." The study of compounds like S-ethyl chloromethanethioate highlights the endless possibilities that the field of chemistry holds!

Synonyms
2941-64-2
Carbonochloridothioic acid, S-ethyl ester
Ethyl chlorothiolformate
S-Ethyl chlorothioformate
Ethyl thiochloroformate
S-Ethyl chlorothiocarbonate
S-(Ethyl)chlorothioformic acid
Ethylthiol chloroformate
S-Ethyl carbonochloridothioate
Ethylthiocarbonyl chloride
S-Ethyl thiochloroformate
S-ETHYL CHLOROTHIOLFORMATE
Thioethoxycarnonyl chloride
Formic acid, chlorothio-, S-ethyl ester
CCRIS 4642
HSDB 5906
Thioethoxycarbonyl chloride
EINECS 220-928-1
UN2826
8B294Z76EO
Ethyl chlorothioloformate
EC 220-928-1
S-ETHYL CHLOROTHIOLFORMATE [HSDB]
SEthyl chlorothioformate
SEthyl thiochloroformate
SEthyl chlorothiocarbonate
SEthyl carbonochloridothioate
Ethyl (chlorosulfenyl)formate
S(Ethyl)chlorothioformic acid
Formic acid, chlorothio-, S-ethyl ester (7CI,8CI)
ETHYL (CHLOROTHIO)FORMATE
Formic acid, chlorothio, Sethyl ester
Carbonochloridothioic acid, Sethyl ester
CHLOROTHIOFORMIC ACID ETHYL ESTER
THIOHYPOCHLOROUS ACID, ANHYDROSULFIDE WITH O-ETHYL THIOCARBONATE
CARBONIC ACID, THIO-, ANHYDROSULFIDE WITH THIOHYPOCHLOROUS ACID, ETHYL ESTER
ethyl chlorothioformate
S-ethyl chloromethanethioate
S-Ethyl chlorothioformic acid
DTXSID6025278
S-Ethyl chloridothiocarbonate
UNII-8B294Z76EO
Ethyl thiolchloroformate
S-Ethyl chlorothiol formate
SCHEMBL162412
DTXCID205278
S-Ethyl chloridothiocarbonate #
CHEMBL1379791
S-Ethyl chlorothioformate, 96%
chlorothioformic acid S-ethyl ester
Tox21_201225
NCGC00091793-01
NCGC00091793-02
NCGC00258777-01
CAS-2941-64-2
DB-047578
NS00004186
Ethyl chlorothioformate [UN2826] [Corrosive]
Q27270126