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S-(3-chloropropyl) thiocarbamate

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Identification
Molecular formula
C4H8ClNOS
CAS number
92-49-9
IUPAC name
S-(3-chloropropyl) carbamothioate
State
State
The compound is usually encountered as a liquid at room temperature. It is colorless to light yellow and may have a slight characteristic odor.
Melting point (Celsius)
-1.20
Melting point (Kelvin)
271.95
Boiling point (Celsius)
107.00
Boiling point (Kelvin)
380.15
General information
Molecular weight
153.65g/mol
Molar mass
153.6460g/mol
Density
1.1760g/cm3
Appearence

The compound typically appears as a colorless to light yellow liquid. It may have a slight sulfurous odor characteristic of thiocarbamate compounds.

Comment on solubility

Solubility of S-(3-chloropropyl) carbamothioate

S-(3-chloropropyl) carbamothioate, with its unique structure, presents specific characteristics regarding solubility that might be intriguing. Here are some key aspects:

  • Polarity: The presence of the chloropropyl group suggests enhanced polarity, which can lead to increased solubility in polar solvents such as water.
  • Hydrophilic vs. Hydrophobic: The carbamothioate functional group can exhibit hydrophilic behavior, potentially aiding solvation in aqueous environments.
  • Solvent Compatibility: It may also be soluble in organic solvents like ethanol or acetone due to its organic nature, making it versatile in various applications.
  • Temperature Influence: As with many organic compounds, solubility may increase with temperature, so temperature adjustments could enhance its dissolution.

In conclusion, while the exact solubility can depend on various factors such as concentration and temperature, “the balance of hydrophilic and hydrophobic characteristics can significantly influence the solubility patterns of S-(3-chloropropyl) carbamothioate.” Therefore, it’s essential to conduct specific tests to determine precise solubility in different solvents.

Interesting facts

Interesting Facts about S-(3-chloropropyl) carbamothioate

S-(3-chloropropyl) carbamothioate is a compelling compound that showcases the fascinating world of organosulfur chemistry. This compound belongs to the category of thioesters, which are known for their unique reactivity and versatility in various applications.

Chemical Characteristics

  • Reactivity: As a thioester, S-(3-chloropropyl) carbamothioate is prone to nucleophilic attack, making it suitable for a variety of chemical reactions that involve carbon-sulfur bond formation.
  • Biological Importance: Compounds of this nature can display biological activity and have been studied for their potential use in pharmaceutical applications. They may act as inhibitors or modulators of specific biological pathways.
  • Industrial Application: This compound's structure allows it to be utilized in agrochemicals as a potential herbicide or pesticide, contributing to agricultural efficiency and pest management.

Unique Features

One of the standout characteristics of S-(3-chloropropyl) carbamothioate is its chloropropyl group, which can enhance the compound's ability to target specific enzymes or receptors in biological systems. This feature is often leveraged in the design of new chemical entities for drug development.

Research and Development

The study of S-(3-chloropropyl) carbamothioate has opened avenues for research in fields such as:

  • Medicinal Chemistry
  • Agricultural Biotechnology
  • Environmental Chemistry

As researchers continue to explore the properties and potential applications of this compound, it underscores the importance of organosulfur compounds in both nature and synthetic chemistry. In the words of famous chemist Linus Pauling, "The best way to have a good idea is to have a lot of ideas," and compounds like S-(3-chloropropyl) carbamothioate exemplify that pursuit of knowledge in chemistry!

Synonyms
S-(3-chloropropyl) carbamothioate
17494-72-3
3-Chloropropyl thiocarbamate
3-Chloropropyl thiolcarbamate
Carbamothioic acid, S-(3-chloropropyl) ester
CARBAMIC ACID, THIO-, S-(3-CHLOROPROPYL)ESTER
Carbamothioic acid S-(3-chloropropyl) ester
NSC-220081
NSC 220081
BRN 1903594
KF4ZBM8WHK
WLN: ZVS3G
DTXSID50169914
NSC220081
AKOS006383258
Carbamic acid, S-(3-chloropropyl)ester
Carbamothioic acid s-(3-chloropropyl)ester