Skip to main content

S-propyl chloromethanethioate

ADVERTISEMENT
Identification
Molecular formula
C4H9ClOS
CAS number
6930-94-1
IUPAC name
S-propyl chloromethanethioate
State
State

At room temperature, S-propyl chloromethanethioate is in the liquid state.

Melting point (Celsius)
-50.00
Melting point (Kelvin)
223.15
Boiling point (Celsius)
165.00
Boiling point (Kelvin)
438.15
General information
Molecular weight
140.64g/mol
Molar mass
140.6380g/mol
Density
1.1234g/cm3
Appearence

S-propyl chloromethanethioate is typically a colorless to pale yellow liquid.

Comment on solubility

Solubility of S-propyl chloromethanethioate

S-propyl chloromethanethioate, with the chemical formula C4H9ClOS, exhibits notable characteristics regarding its solubility:

  • It is generally considered to be soluble in organic solvents such as ethanol and acetone.
  • The presence of both a chlorine atom and a thiol group contributes to its polar nature, affecting its solubility behavior.
  • However, its solubility in water is quite limited due to its hydrophobic hydrocarbon chain.

To summarize, while S-propyl chloromethanethioate demonstrates good solubility in organic media, its limited solubility in water makes it a compound better suited for applications within non-aqueous environments. This solubility profile can have significant implications in chemical reactions and formulations where solubility is a critical factor. As with many organic compounds, the solvent choice must align well with the characteristics of the solute for optimal interactions.

Interesting facts

Interesting Facts About S-propyl Chloromethanethioate

S-propyl chloromethanethioate, also known as a thioester, is a fascinating compound that belongs to the family of organosulfur compounds. Here are some highlights and intriguing aspects of this compound:

  • Unique Structure: This compound features a sulfur atom, which plays a critical role in its reactivity and interaction with other molecules. The presence of the thiol (–SH) group makes it distinct among other chlorinated solvents.
  • Biochemical Relevance: Thioesters, including S-propyl chloromethanethioate, are significant in biological systems because they participate in important enzymatic reactions, particularly in the synthesis of fatty acids and the metabolism of amino acids.
  • Industrial Applications: This compound may be used as an intermediate in the synthesis of various chemicals, highlighting its utility in producing other valuable compounds in both research and industry.
  • Environmental Considerations: Understanding the behavior and fate of organosulfur compounds like S-propyl chloromethanethioate is crucial for assessing their impact on the environment and exploring ways to minimize potential risks.
  • Research Potential: The unique properties of S-propyl chloromethanethioate make it a subject of interest in organic synthesis and materials science, leading to ongoing research into new applications and properties.

As a compound that bridges both organic chemistry and biochemistry, S-propyl chloromethanethioate presents numerous avenues for exploration, emphasizing the interconnectedness of chemical science and its applications in various fields. Remember, as with all chemical substances, proper safety precautions should be considered when handling or studying them!

Synonyms
S-PROPYL CHLOROTHIOFORMATE
Propyl chlorothioformate
Carbonochloridothioic acid, S-propyl ester
n-Propyl thiochloroformate
S-(n-propyl)chlorothioformic acid
Propyl chlorothiolformate
n-Propyl chlorothiolformate
CCRIS 6097
HSDB 6155
S-(n-Propyl) carbonochloridothioate
EINECS 237-656-4
NSC 72086
BRN 1633747
AI3-52665
NSC-72086
S-PROPYL CHLOROTHIOFORMATE [HSDB]
nPropyl chlorothioformate
nPropyl thiochloroformate
SPropyl thiochloroformate
nPropyl chlorothiolformate
n-Propyl chlorothiolformate.
S(nPropyl) thiochloroformate
1-Propyl chlorothiolformate.
S(Propyl)chlorothioformic acid
S-propyl carbonochloridothioate
S(nPropyl) carbonochloridothioate
S-(n-propyl) thiochloroformate.
S-(n-propyl) carbonochloridothioate.
Formic acid, chlorothio, Spropyl ester
Carbonochloridothioic acid, Spropyl ester
n-Propyl chlorothioformate
13889-92-4
S-Propyl thiochloroformate
S-propyl chloromethanethioate
S-(n-Propyl) thiochloroformate
S-(Propyl)chlorothioformic acid
Formic acid, chlorothio-, S-propyl ester
S-(Propyl) chlorothioformate
S8YPJ4718Q
DTXSID8025963
S-Propyl chloridothiocarbonate
UNII-S8YPJ4718Q
(Propylthio)carbonyl chloride
Formic acid, S-propyl ester
S-propyl carbon-chloridothioate
DTXCID305963
SCHEMBL1085613
s-Propyl chlorothioformate,96%
CHEMBL1469099
S-Propyl chloridothiocarbonate #
S-Propyl chlorothioformate, 96%
NSC72086
Tox21_202532
AKOS024319089
NCGC00091828-01
NCGC00260081-01
BS-21379
CAS-13889-92-4
DB-042455
NS00024494
Q27289063