Skip to main content

Baygon

ADVERTISEMENT
Identification
Molecular formula
C13H10ClNO2
CAS number
101-20-2
IUPAC name
(3-chlorophenyl) N-phenylcarbamate
State
State

At room temperature, (3-Chlorophenyl) N-phenylcarbamate is typically found in a solid state. This is common for many carbamates which often exhibit a higher degree of thermal stability and remain solid at ambient conditions.

Melting point (Celsius)
61.00
Melting point (Kelvin)
334.00
Boiling point (Celsius)
356.00
Boiling point (Kelvin)
629.00
General information
Molecular weight
249.69g/mol
Molar mass
249.6850g/mol
Density
1.3000g/cm3
Appearence

(3-Chlorophenyl) N-phenylcarbamate appears as a white crystalline solid. It is characterized by its specific crystalline structure that is typical of many organic compounds including various carbamates. The compound maintains a unique structure due to the presence of a chlorine atom on the phenyl ring, which can slightly affect its crystal packing and appearance.

Comment on solubility

Solubility of (3-chlorophenyl) N-phenylcarbamate

The solubility of (3-chlorophenyl) N-phenylcarbamate can be influenced by several factors, primarily its chemical structure and the environmental conditions it encounters. Here are some key points to consider:

  • Polarity: As a carbamate derivative, the compound exhibits polar characteristics due to the presence of the carbamate functional group. This may promote some degree of solubility in polar solvents.
  • Solvent Compatibility: Common solvents such as water, alcohols, and acetone may interact differently with (3-chlorophenyl) N-phenylcarbamate. For example:
    • In water: Its solubility can be limited due to relatively low polarity.
    • In alcohols: It might exhibit enhanced solubility owing to favorable interactions with the alkyl groups.
    • In aromatic hydrocarbons: The compound could demonstrate higher solubility due to structural compatibility.
  • Temperature Effects: Increased temperature often improves solubility. Hence, testing solubility at varying temperatures could yield significant insights.
  • pH Influence: The solubility may vary with pH changes, affecting the ionization of functional groups, especially in aqueous solutions.

In summary, understanding the solubility of (3-chlorophenyl) N-phenylcarbamate requires a comprehensive analysis of its physical and chemical properties as well as the solvent environment. This analysis is crucial for its application in various chemical processes and formulations.

Interesting facts

Interesting Facts about (3-chlorophenyl) N-phenylcarbamate

(3-chlorophenyl) N-phenylcarbamate is a fascinating compound that has garnered attention in various fields, particularly in agriculture and medicine. Here are some intriguing highlights about this chemical:

  • Insecticide Properties: This compound exhibits notable insecticidal activity, making it an important candidate in pest control formulations.
  • Herbicide Potential: Beyond its insect repellency, it is being studied for its potential use as a herbicide, helping to manage unwanted vegetation effectively.
  • Medical Applications: Due to its unique structure, (3-chlorophenyl) N-phenylcarbamate is also explored for potential use in pharmaceuticals, particularly as a template for developing new drugs.
  • Structure Activity Relationship: The presence of the chlorine atom on the phenyl ring improves the bioactivity of the compound, showcasing the importance of molecular modification in enhancing chemical properties.
  • Environmental Impact: Researchers are investigating the environmental impact of this compound, especially concerning its degradation products and persistence in ecosystems.

As scientists continue to explore the capabilities of (3-chlorophenyl) N-phenylcarbamate, it stands as a prime example of how a single compound can have multifaceted applications across different domains. Understanding such compounds paves the way for innovative solutions to modern challenges in agriculture and healthcare.

Synonyms
M-CHLOROPHENYL CARBANILATE
16400-09-2
Cambridge id 5141861
DTXSID20167689
HMS1757P15
AKOS001027152
Z55290734