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Fenobucarb

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Identification
Molecular formula
C12H17NO2
CAS number
3766-81-2
IUPAC name
(3-tert-butylphenyl) N-methylcarbamate
State
State

Fenobucarb is a liquid at room temperature.

Melting point (Celsius)
0.50
Melting point (Kelvin)
273.65
Boiling point (Celsius)
130.00
Boiling point (Kelvin)
403.15
General information
Molecular weight
193.25g/mol
Molar mass
193.2500g/mol
Density
1.0300g/cm3
Appearence

Fenobucarb typically appears as a colorless to yellowish liquid. It may have a slight characteristic odor, commonly associated with many carbamate pesticides.

Comment on solubility

Solubility of (3-tert-butylphenyl) N-methylcarbamate

(3-tert-butylphenyl) N-methylcarbamate presents an intriguing case when it comes to its solubility characteristics. As a carbamate compound, its solubility can be influenced by several factors related to both the molecular structure and external conditions.

Key Factors Affecting Solubility:

  • Molecular Polarities: The presence of polar functional groups, such as the carbamate moiety, generally enhances solubility in polar solvents.
  • Hydrophobic Interactions: The tert-butyl group contributes to hydrophobic character, potentially decreasing solubility in water.
  • Temperature Influences: Increased temperature often improves solubility, allowing the compound to preferentially dissolve in suitable solvents.

In summary, the solubility of (3-tert-butylphenyl) N-methylcarbamate can be best described with the phrase: “It depends.” Depending on the solvent used and temperature, it can exhibit varying degrees of solubility. For instance:

  • In water, the solubility may be limited due to the hydrophobic nature of the tert-butyl group.
  • In more polar organic solvents, one can expect relatively higher solubility values.

As with many organic compounds, understanding the solubility of (3-tert-butylphenyl) N-methylcarbamate requires a nuanced approach that considers the balance between its polar and non-polar components.

Interesting facts

Interesting Facts about (3-tert-butylphenyl) N-methylcarbamate

(3-tert-butylphenyl) N-methylcarbamate is a fascinating compound that falls under the category of carbamates, which are esters or salts of carbamic acid. Here are some key points that make this compound noteworthy:

  • Application in Agriculture: Carbamates like this compound are often utilized as *pesticides* and *herbicides*, making them vital in agricultural practices to protect crops from pests.
  • Mechanism of Action: The efficacy of this compound can be attributed to its mechanism of inhibiting *acetylcholinesterase*, an enzyme crucial for nerve function in pests. This makes it effective in controlling pest populations.
  • Safety Considerations: Despite its usefulness, it is essential to handle (3-tert-butylphenyl) N-methylcarbamate with care. Many carbamate compounds can pose risks to non-target organisms, including humans.
  • Research Applications: In the field of organic chemistry, studies on carbamates, including this one, help researchers develop *safer* and *more efficient* compounds, enhancing sustainable agricultural techniques.
  • Structural Features: The presence of the tert-butyl group in the structure contributes to the compound's stability and affects its *lipophilicity*, which plays a significant role in its biological activity.

In summary, (3-tert-butylphenyl) N-methylcarbamate exemplifies the complexity and utility of carbamate compounds. As researchers continue to explore its properties and applications, this compound stands as a testament to the intricate relationship between chemistry and agricultural technology.

Synonyms
Terbam
Knockbal
3-tert-Butylphenyl N-methylcarbamate
EINECS 212-303-7
RE 5030
BRN 1876800
Phenol, 3-(1,1-dimethylethyl)-, methylcarbamate
3-(1,1-Dimethylethyl)phenol methylcarbamate
4-06-00-03295 (Beilstein Handbook Reference)
CARBAMIC ACID, METHYL-, 3-tert-BUTYLPHENYL ESTER
Phenol, 3-(1,1-dimethylethyl)-, 1-(N-methylcarbamate)
m-tert-Butylphenyl methylcarbamate
780-11-0
(3-tert-butylphenyl) N-methylcarbamate
CHEMBL2046821
3-Tert-Butylphenyl Methylcarbamate
TBPMC
SCHEMBL78061
DTXSID80876907
FSJYRLHKLVGCNH-UHFFFAOYSA-N
BDBM50064476
M-T-BUTYLPHENYL N-METHYLCARBAMATE
NS00042216
Phenol,3-(1,1-dimethylethyl)-,1-(N-methylcarbamate)