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Phenmedipham

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Identification
Molecular formula
C9H10N2O2
CAS number
122-42-9
IUPAC name
(2-cyanophenyl) N-methylcarbamate
State
State

At room temperature, (2-cyanophenyl) N-methylcarbamate is typically in a solid state, manifesting as crystalline or a powder. It is stable under normal conditions of temperature and pressure.

Melting point (Celsius)
99.00
Melting point (Kelvin)
372.15
Boiling point (Celsius)
336.50
Boiling point (Kelvin)
609.65
General information
Molecular weight
178.19g/mol
Molar mass
178.1960g/mol
Density
1.2100g/cm3
Appearence

(2-cyanophenyl) N-methylcarbamate appears as a colorless to pale yellow crystalline solid. It may also be encountered as an off-white powder depending on its purity and method of preparation.

Comment on solubility

Solubility of (2-cyanophenyl) N-methylcarbamate

The solubility of (2-cyanophenyl) N-methylcarbamate can be assessed by considering several factors that influence its dissolution in various solvents. The solubility characteristics of this compound can be summarized as follows:

  • Polarity: Due to its cyanophenyl group and carbamate structure, (2-cyanophenyl) N-methylcarbamate exhibits moderate polarity, which may enhance its solubility in polar solvents such as water and methanol.
  • Hydrogen Bonding: The carbamate functional group allows for potential hydrogen bonding with solvents, which further increases the likelihood of solubility in polar environments.
  • Solvent Compatibility: Solubility tends to be higher in solvents like dimethyl sulfoxide (DMSO) or dimethylformamide (DMF), suggesting that this compound is more soluble in aprotic polar solvents compared to protic ones.
  • Temperature Effects: As with many chemical compounds, an increase in temperature typically enhances solubility. Thus, (2-cyanophenyl) N-methylcarbamate may dissolve more readily at elevated temperatures.

In summary, while (2-cyanophenyl) N-methylcarbamate demonstrates favorable solubility characteristics in polar solvents due to its structure, empirical testing is essential for precise solubility values in specific conditions. As with any compound, understanding its solubility profile is vital for applications in synthesis or formulation. Remember, "solubility is the key to accessibility!"

Interesting facts

Interesting Facts about (2-cyanophenyl) N-methylcarbamate

(2-cyanophenyl) N-methylcarbamate is a fascinating chemical compound that belongs to the class of carbamates, which are notable for their applications in various fields, including agriculture and pharmaceuticals. Here are some intriguing points about this compound:

  • Biological Activity: This compound exhibits interesting biological properties, making it a subject of study for its potential use as an insecticide and herbicide.
  • Structure Insights: The molecular structure features a cyanophenyl group, which enhances the electronic properties, allowing it to interact effectively with biological receptors.
  • Synthetic Pathways: The synthesis of (2-cyanophenyl) N-methylcarbamate can be achieved through various methods, often involving the reaction of cyanophenol derivatives with methyl isocyanate.
  • Environmental Considerations: As with many chemical compounds, there are ongoing studies focused on understanding the environmental impact and degradation pathways of this carbamate in soil and water.
  • Role in Research: This compound is often used as a model compound in research aimed at understanding the behavior of carbamate pesticides, providing insights into their efficacy and safety.

Moreover, the **N-methyl** component contributes to the compound's ability to permeate biological membranes, enhancing its potential effectiveness in target applications. As researchers continue to investigate (2-cyanophenyl) N-methylcarbamate, it remains an important compound within the realm of chemical studies.

In the words of a renowned chemist, "Understanding the intricate details of chemical compounds like this is pivotal in crafting solutions that align with ecological sustainability."


Synonyms
Salicylonitrile methylcarbamate
942-79-0
2-Cyanophenyl N-methylcarbamate
BRN 2839189
2-(((Methylamino)carbonyl)oxy)benzonitrile
Carbamic acid, methyl-, ester with salicylonitrile
DTXSID70240971
BENZONITRILE, 2-(((METHYLAMINO)CARBONYL)OXY)-
DTXCID00163462
CHEMBL3249280
SCHEMBL26135692