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fenobucarb

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Identification
Molecular formula
C12H17NO2
CAS number
3766-81-2
IUPAC name
[3-(1-ethylpropyl)phenyl] N-methylcarbamate
State
State

At room temperature, fenobucarb can be found in both solid and liquid states, depending on the specific environmental conditions. It is mostly a crystalline solid near room temperature or higher due to its relatively low melting point of 13.2°C.

Melting point (Celsius)
13.20
Melting point (Kelvin)
286.35
Boiling point (Celsius)
324.00
Boiling point (Kelvin)
597.15
General information
Molecular weight
207.28g/mol
Molar mass
207.2650g/mol
Density
1.0453g/cm3
Appearence

Fenobucarb is a liquid or crystalline solid, depending on the ambient temperature. It is usually clear and colorless but can appear as a light yellow due to certain impurities or reactions with air over time. It may not have a significant odor in pure form but is characterized by its potential to form a visible shine or sheen on surfaces.

Comment on solubility

Solubility of [3-(1-ethylpropyl)phenyl] N-methylcarbamate

The solubility of [3-(1-ethylpropyl)phenyl] N-methylcarbamate is an intriguing aspect to consider, particularly in various solvents. Its solubility can be influenced by several factors, including temperature, pH, and the nature of the solvent. Here are some essential points to note:

  • Polar solvents: This compound is more likely to be soluble in polar solvents due to the presence of the carbamate functional group, which can engage in hydrogen bonding.
  • Non-polar solvents: Given its phenyl and ethylpropyl groups, [3-(1-ethylpropyl)phenyl] N-methylcarbamate may demonstrate reasonable solubility in non-polar solvents, though it may not be as high as in polar solvents.
  • Temperature: As with many organic compounds, increasing the temperature generally enhances solubility, allowing for greater interaction between solute and solvent particles.

Furthermore, it is essential to consider that solubility can also be expressed quantitatively, often in units such as grams per liter (g/L). For this compound, experimental data might vary, emphasizing the need for empirical studies to elucidate precise solubility parameters.

In summary, the solubility profile of [3-(1-ethylpropyl)phenyl] N-methylcarbamate is largely governed by its molecular structure and the interacting solvents. Understanding these solubility characteristics is crucial for its application in chemical synthesis, formulation, and environmental behavior.

Interesting facts

Interesting Facts About [3-(1-ethylpropyl)phenyl] N-methylcarbamate

[3-(1-ethylpropyl)phenyl] N-methylcarbamate is a fascinating compound with a variety of applications and properties that have garnered attention in the fields of chemistry and biotechnology.

Key Features:

  • Structure and Functionality: This compound features a carbamate functional group, which is known for its versatility in organic synthesis and use in pharmaceutical applications.
  • Biological Activity: Compounds that contain N-methylcarbamates are often studied for their potential insecticidal and herbicidal effects, as they can inhibit the activity of essential enzymes in pests and weeds.
  • Synthetic Pathways: The synthesis of this compound involves the reaction between isocyanates and alcohols. This highlights the importance of green chemistry principles, as many reactions can be optimized to reduce waste and increase efficiency.
  • Research Potential: The unique structure of [3-(1-ethylpropyl)phenyl] N-methylcarbamate makes it a compound of interest for drug discovery and development. Researchers are investigating its ability to interact with specific biological targets.
  • Environmental Considerations: As with many carbamate derivatives, it’s important to understand the environmental impact and metabolic pathways, ensuring that the benefits of its application do not outweigh potential ecological repercussions.

As a chemistry student or scientist, it’s crucial to realize the significance of compounds like [3-(1-ethylpropyl)phenyl] N-methylcarbamate in drug development and agricultural chemistry. The continual study of such compounds not only enhances our understanding of chemistry but also paves the way for innovations that can lead to the development of more effective and sustainable solutions in various industries.

Synonyms
M-(1-ETHYLPROPYL)PHENYL METHYLCARBAMATE
3-(1-Ethylpropyl)phenyl Methylcarbamate
UNII-XKB1UJJ0WL
XKB1UJJ0WL
HSDB 2589
DTXSID1042102
M-(1-ETHYLPROPYL)PHENYL METHYLCARBAMATE [HSDB]
PHENOL, 3-(1-ETHYLPROPYL)-, 1-(N-METHYLCARBAMATE)
DTXCID4020323
Phenol, m(1ethylpropyl), methylcarbamate
Phenol, 3(1ethylpropyl), methylcarbamate
3-(1-Ethylpropyl)phenyl methylcarbamic acid
Phenol, m(1ethylpropyl), methylcarbamate (8CI)
Carbamic acid, methyl, m(1ethylpropyl)phenyl ester
N-methyl-1-3-(pentan-3-yl)phenoxymethanimidic acid
bux-ten
metalcamat
metalkamate
672-04-8
(3-pentan-3-ylphenyl) N-methylcarbamate
Carbamic acid, methyl-, m-(1-ethylpropyl)phenyl ester
3-(pentan-3-yl)phenyl N-methylcarbamate
Phenol, m-(1-ethylpropyl)-, methylcarbamate
3-(1-Ethylpropyl)phenol 1-(N-Methylcarbamate); Methylcarbamic Acid m-(1-Ethylpropyl)phenyl Ester; m-(1-Ethylpropyl)phenol Methylcarbamate; m-(1-Ethylpropyl)phenyl Methylcarbamate;
Phenol, 3-(1-ethylpropyl)-, methylcarbamate
SCHEMBL5933894
(3-Pentan-3-ylphenyl)n-methylcarbamate
3-(1-ethylpropyl) phenylmethyl carbamate
DB-303681
NS00005303
Q27293877