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Carbaryl

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Identification
Molecular formula
C12H11NO2
CAS number
63-25-2
IUPAC name
[3-(methoxycarbonylamino)phenyl] N-methylcarbamate
State
State

At room temperature, Carbaryl is typically found in a solid crystalline state.

Melting point (Celsius)
142.00
Melting point (Kelvin)
415.15
Boiling point (Celsius)
150.00
Boiling point (Kelvin)
423.15
General information
Molecular weight
201.22g/mol
Molar mass
201.2200g/mol
Density
1.2330g/cm3
Appearence

Carbaryl appears as a colorless to white crystalline solid. It is often sold as a powder and may have a slight chemical odor.

Comment on solubility

Solubility Characteristics of [3-(methoxycarbonylamino)phenyl] N-methylcarbamate

The solubility of [3-(methoxycarbonylamino)phenyl] N-methylcarbamate can be influenced by a variety of factors, including temperature, pH, and the presence of other solutes. Here are key points to consider:

  • Polarity: This compound contains functional groups that may contribute to its polar characteristics, potentially enhancing its solubility in polar solvents such as water or methanol.
  • Hydrogen Bonding: The ability to form hydrogen bonds due to amine and ester groups suggests increased solubility in aqueous environments.
  • Temperature Dependence: As with many organic compounds, the solubility is likely to increase with temperature, making it more soluble in warm solvents.
  • pH Sensitivity: The solubility may also be affected by the pH of the solution, particularly if the compound ionizes at different pH levels.

In summary, the solubility of [3-(methoxycarbonylamino)phenyl] N-methylcarbamate is expected to be greater in polar solvents and influenced by environmental factors. To investigate its precise solubility, empirical testing under controlled conditions is essential.

Interesting facts

Interesting Facts about 3-(Methoxycarbonylamino)phenyl N-methylcarbamate

3-(Methoxycarbonylamino)phenyl N-methylcarbamate is an intriguing compound with applications in various scientific fields, particularly in medicinal chemistry. Here are some fascinating highlights:

  • Pharmaceutical Potential: This compound acts as an important intermediate in the synthesis of more complex pharmaceuticals, often aiming to enhance therapeutic efficacy and reduce side effects.
  • Structural Features: The presence of both methoxycarbonyl and carbamate functional groups contributes to its chemical reactivity, making it a versatile building block for drug development.
  • Mechanism of Action: This compound may serve as an inhibitor in certain enzymatic pathways, a feature studied for developing therapies against diseases such as cancer and various infections.
  • Identification and Analysis: Advanced spectroscopic techniques such as NMR and mass spectrometry are used to characterize this compound, showcasing the importance of analytical chemistry in compound development.
  • Environmental Considerations: The stability and breakdown of carbamates in natural environments are crucial for assessing ecological impacts, underlining the need for responsible usage and thorough environmental studies.

In summary, 3-(methoxycarbonylamino)phenyl N-methylcarbamate serves not only as an interesting subject of study due to its structural characteristics but also as a crucial component that can lead to novel therapeutic developments. As scientists continue to explore its properties and effects, we may uncover even more valuable applications in medicine and biology.

Synonyms
13684-67-8
CARBANILIC ACID, m-HYDROXY-, METHYL ESTER, METHYLCARBAMATE
Methyl m-hydroxycarbanilate, methylcarbamate
BRN 2418760
m-Hydroxycarbanilic acid methyl ester methylcarbamate
DTXSID30159974
DTXCID3082465
[3-(methoxycarbonylamino)phenyl] N-methylcarbamate
Methyl (3-((methylcarbamoyl)oxy)phenyl)carbamate
starbld0042772
orb1986292
AKOS040751021