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Chlorpropham

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Identification
Molecular formula
C10H12ClNO2
CAS number
101-21-3
IUPAC name
methyl N-(2-chlorophenyl)carbamate
State
State

At room temperature, Chlorpropham is in a solid state.

Melting point (Celsius)
41.00
Melting point (Kelvin)
314.15
Boiling point (Celsius)
400.00
Boiling point (Kelvin)
673.15
General information
Molecular weight
213.66g/mol
Molar mass
213.6600g/mol
Density
1.3900g/cm3
Appearence

Chlorpropham is a colorless to white crystalline solid. It appears as a solid at room temperature and is often powdered in form.

Comment on solubility

Solubility of Methyl N-(2-chlorophenyl)carbamate

Methyl N-(2-chlorophenyl)carbamate, a carbamate derivative, exhibits unique solubility characteristics that are essential for its applications. Understanding the solubility of this compound is crucial for various chemical processes and formulations. Below are some key points regarding its solubility:

  • Polarity: Methyl N-(2-chlorophenyl)carbamate has a combination of polar and non-polar functional groups, which can influence its solubility in different solvents.
  • Solvent Compatibility: This compound is generally more soluble in organic solvents, such as:
    • Ethyl acetate
    • Dimethyl sulfoxide (DMSO)
    • Acetone
  • Water Solubility: The solubility in water is expected to be limited due to the non-polar character of the aromatic ring, though it may show some degree of solubility depending on pH and temperature conditions.
  • Temperature Influence: As with many compounds, increasing temperature typically enhances solubility, allowing for higher concentrations of methyl N-(2-chlorophenyl)carbamate in solution.

In conclusion, while methyl N-(2-chlorophenyl)carbamate demonstrates a tendency toward solubility in organic solvents, its performance in aqueous environments may not be as favorable. Consequently, exploration of suitable solvents is imperative for effective utilization in practical applications.

Interesting facts

Interesting Facts about Methyl N-(2-chlorophenyl)carbamate

Methyl N-(2-chlorophenyl)carbamate is a fascinating compound that falls under the category of carbamate pesticides. This compound has garnered attention not only for its utility in agricultural applications but also for its chemical properties. Here are some intriguing aspects of this compound:

  • Biological Activity: This compound exhibits significant biological activity, making it an important player in the field of agrochemicals. It functions as a pesticide, providing a means of protecting crops from both insects and weeds.
  • Mechanism of Action: Methyl N-(2-chlorophenyl)carbamate works by inhibiting the activity of certain enzymes in insects, leading to the disruption of vital processes like neurotransmission. This unique mode of action helps in controlling pest populations effectively.
  • Environmental Impact: As with many pesticides, understanding the environmental impact is crucial. Research into the degradation pathways of carbamates, including this compound, highlights the importance of responsible usage to minimize ecological disturbance.
  • Pharmaceutical Relevance: Beyond its agricultural application, compounds similar to methyl N-(2-chlorophenyl)carbamate have been studied for potential therapeutic uses, particularly in medicinal chemistry where their structural similarities can lead to novel drug design.
  • Synthesis: The synthesis of methyl N-(2-chlorophenyl)carbamate involves the reaction of the corresponding amine with carbonyl compounds, showcasing the versatility of organic reactions in creating useful chemicals.

In summary, methyl N-(2-chlorophenyl)carbamate is not only significant for its use in pest control but also for its broader implications in environmental science and medicinal research. Researchers continue to explore its properties and potential applications, making it a compound of interest in various scientific fields.

Synonyms
methyl N-(2-chlorophenyl)carbamate
UNII-UKU5YTI0XJ
HSDB 2755
CARBANILIC ACID, O-CHLORO-, METHYL ESTER
methyl O-chlorocarbanilate
Methyl 2-chlorophenylcarbamate
Carbamic acid, (2-chlorophenyl)-, methyl ester
METHYL 2-CHLOROCARBANILATE
Carbamic acid, (o-chlorophenyl)-, methyl ester
DTXSID00174710
METHYL (O-CHLOROPHENYL)CARBAMATE
CARBAMIC ACID, N-(2-CHLOROPHENYL)-, METHYL ESTER
CARBAMIC ACID, (O-CHLOROPHENYL)-, METHYL ESTER [HSDB]
DTXCID4097201
Carbamic acid, (ochlorophenyl), methyl ester
Carbamic acid, (2chlorophenyl), methyl ester
RefChem:123476
20668-13-7
methyl (2-chlorophenyl)carbamate
UKU5YTI0XJ
SCHEMBL513877
SCHEMBL513878
methyl-2-chlorophenyl-carbamate
Methyl 2-chlorophenylcarbamate #
SJTVPRCAJODHGA-UHFFFAOYSA-N
N-(2-chlorophenyl)methoxycarboxamide
STK490036
AKOS003247429
HS-3685
DA-43303
CS-0336497
ST50549941
Q27291123
F3035-0954