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Chlorbufam

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Identification
Molecular formula
C9H9Cl2NO1S1
CAS number
133-85-1
IUPAC name
S-(4-chlorophenyl) N-(2-chloroethyl)carbamothioate
State
State

Chlorbufam is typically in a solid state at room temperature.

Melting point (Celsius)
45.00
Melting point (Kelvin)
318.15
Boiling point (Celsius)
329.00
Boiling point (Kelvin)
602.15
General information
Molecular weight
235.15g/mol
Molar mass
235.0900g/mol
Density
1.3300g/cm3
Appearence

Chlorbufam appears as a colorless or slightly yellow crystalline solid. It is sometimes encountered in powder form with a faint characteristic odor.

Comment on solubility

Solubility of S-(4-chlorophenyl) N-(2-chloroethyl)carbamothioate

S-(4-chlorophenyl) N-(2-chloroethyl)carbamothioate is a compound that exhibits interesting solubility properties. Understanding its solubility can shed light on its potential applications and behavior in various environments.

Solubility Characteristics

This compound is generally characterized by:

  • Moderate Solubility: S-(4-chlorophenyl) N-(2-chloroethyl)carbamothioate shows moderate solubility in polar solvents, particularly in water and alcohols.
  • Limited Solubility in Non-Polar Solvents: It tends to be less soluble in non-polar solvents due to its polar functional groups.
  • Temperature Dependence: The solubility may increase with temperature, indicating that heat may facilitate dissolving the compound in solvent systems.

In summary, the solubility of S-(4-chlorophenyl) N-(2-chloroethyl)carbamothioate is influenced by various factors, which include:

  1. Type of solvent used
  2. Temperature conditions
  3. Concentration levels

As stated, "Understanding solubility is vital," especially for applications in pharmacology and environmental science where the compound's behavior in different phases must be predicted accurately. Thus, grasping the solubility characteristics of this compound is crucial for its effective use and management.

Interesting facts

Interesting Facts about S-(4-chlorophenyl) N-(2-chloroethyl)carbamothioate

S-(4-chlorophenyl) N-(2-chloroethyl)carbamothioate is a fascinating chemical compound that belongs to the group of organophosphates, playing significant roles in agricultural and biological sciences. This compound engages the interest of researchers for several compelling reasons:

  • Pesticide Properties: This compound is primarily used as a pesticide, demonstrating effective insecticidal properties that are crucial for crop protection.
  • Mechanism of Action: The way this compound interacts with pests is quite notable. It typically inhibits a critical enzyme called acetylcholinesterase, leading to a buildup of acetylcholine, causing paralysis and death in insects.
  • Synthesis and Applications: The synthesis of S-(4-chlorophenyl) N-(2-chloroethyl)carbamothioate can involve a variety of chemical reactions, including nucleophilic substitution. Its applications extend beyond agriculture, as it is also studied for potential use in chemical biology.
  • Environmental Considerations: While effective against pests, there are ongoing discussions regarding the environmental impact of using this compound. Research is being conducted to assess its safety and to promote sustainable agricultural practices.

In the words of a prominent chemist, “Understanding the breadth of organophosphate compounds sows the seeds for innovations in pest management, influencing both the economy and ecology.” Thus, S-(4-chlorophenyl) N-(2-chloroethyl)carbamothioate not only enriches our knowledge of chemistry but also poses significant questions regarding its safe usage.

In summary, this compound exemplifies the fusion of chemical science and agricultural technology, presenting a mixture of challenges and opportunities for scientists and farmers alike.

Synonyms
22039-90-3
2-Chloroethylthiocarbamic acid, S-p-chlorophenyl ester
NSC 160179
BRN 2525524
DTXSID80176510
CARBAMIC ACID, (2-CHLOROETHYL)THIO-, S-p-CHLOROPHENYL ESTER
(2-Chloroethyl)-thiocarbamic acid p-chlorophenyl ester
RefChem:331935
DTXCID2099001
NSC160179
NSC-160179
DS-007413
CARBAMIC ACID,(2-CHLOROETHYL)THIO-, S-(P-CHLOROPHENYL) ESTER (8CI)