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Phenyl N-methylcarbamate

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Identification
Molecular formula
C8H9NO2
CAS number
557-14-8
IUPAC name
methyl N-phenylcarbamate
State
State

In its pure form, methyl N-phenylcarbamate is a solid at room temperature.

Melting point (Celsius)
46.00
Melting point (Kelvin)
319.15
Boiling point (Celsius)
290.00
Boiling point (Kelvin)
563.15
General information
Molecular weight
151.17g/mol
Molar mass
151.1650g/mol
Density
1.1970g/cm3
Appearence

Methyl N-phenylcarbamate is typically a colorless crystalline solid or white powder.

Comment on solubility

Solubility of Methyl N-phenylcarbamate

Methyl N-phenylcarbamate, with the chemical formula C9H10N2O2, exhibits interesting solubility characteristics that are important for its applications in various fields. The solubility of this compound can be influenced by factors such as temperature and the specific solvent used. Here are some key points regarding its solubility:

  • Solvent Interaction: Methyl N-phenylcarbamate is more soluble in organic solvents compared to water, due to its non-polar aromatic structure.
  • Temperature Dependency: Like many organic compounds, solubility often increases with temperature, making it easier to dissolve in hotter solvents.
  • Polarity Consideration: The balance of polar and non-polar groups within the molecule suggests that it will have limited solubility in highly polar solvents.
  • Practical Applications: Understanding solubility aids in the formulation of this compound in pharmaceuticals and agricultural products.

In conclusion, methyl N-phenylcarbamate's solubility behavior reflects its structural properties. As many chemists say, "Solubility is the key to understanding reactivity and application in formulations." This highlights the need for a well-rounded knowledge of solubility to optimize its use in various processes.

Interesting facts

Intriguing Facts About Methyl N-phenylcarbamate

Methyl N-phenylcarbamate is a fascinating compound that garners the interest of both chemists and biochemists alike. This compound belongs to the family of carbamates, which are known for their versatility in various applications. Here are some key points that highlight its significance:

  • Pharmaceutical Applications: Methyl N-phenylcarbamate has been explored for its potential pharmacological effects. It may act as a metabolic intermediary in key biochemical pathways.
  • Insecticidal Properties: Compounds like methyl N-phenylcarbamate can exhibit biological activity, which makes them valuable in agriculture as insecticides and pest control agents.
  • Chemical Stability: One of the impressive features of this compound is its stability under various conditions, allowing it to be utilized effectively in formulations.
  • Synthetic Versatility: The synthetic methods to obtain methyl N-phenylcarbamate can vary, showcasing the ingenious techniques chemists can employ to manipulate molecular structures.

This compound also serves as an intriguing subject for students delving into the study of organic chemistry. Its structure imparts various properties that are critical in understanding reactivity patterns.

As the renowned chemist Marie Curie once said, “All human beings should be able to receive education that allows them to think critically and innovate.” Methyl N-phenylcarbamate is a perfect example of a compound that encourages critical thinking in organic synthesis and application.

In summary, methyl N-phenylcarbamate not only presents diverse applications but also illustrates the intricate connections between chemical compounds and their practical uses in our everyday life.

Synonyms
METHYL N-PHENYLCARBAMATE
Methyl phenylcarbamate
N-Phenylcarbamic acid methyl ester
Methyl carbanilate
Methyl phenylurethane
Carbamic acid, N-phenyl-, methyl ester
Methyl N-phenylurethane
Carbanilic acid, methyl ester
Carbamic acid, phenyl-, methyl ester
B3L1HPI8NJ
UNII-B3L1HPI8NJ
NSC-36208
METHANOL CARBANILATE
phenylcarbamic acid methyl ester
Carbamic acid, phenyl-, methyl ester (9CI)
IAGUPODHENSJEZ-UHFFFAOYSA-
N-PHENYL-O-METHYLURETHANE
DTXSID00180674
N-(METHOXYCARBONYL)ANILINE
O-METHYL N-PHENYLCARBAMATE
EINECS 220-014-2
NSC 36208
AI3-15077
DTXCID40103165
Carbanilic acid, methyl ester (8CI)
220-014-2
iagupodhensjez-uhfffaoysa-n
inchi=1/c8h9no2/c1-11-8(10)9-7-5-3-2-4-6-7/h2-6h,1h3,(h,9,10)
2603-10-3
MFCD00027552
N-phenyl-carbamic acid methyl ester
Carbamic acid,N-phenyl-, methyl ester
methyl phenyl carbamate
SCHEMBL282531
CHEMBL4529032
HMS1721H14
methyl hydrogen phenylimidocarbonate
N-phenyl carbamic acid methyl ester
NSC36208
STK397155
AKOS000119957
AS-63536
SY053927
DB-046821
CS-0066443
NS00046786
P1010
EN300-16865
D70137
Z56801320