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Carbaryl

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Identification
Molecular formula
C12H11NO2
CAS number
63-25-2
IUPAC name
O-(2-naphthyl) N-methyl-N-(1-naphthyl)carbamothioate
State
State

At room temperature, Carbaryl is typically in a solid state. It is stable and mainly encountered in its crystalline form.

Melting point (Celsius)
142.00
Melting point (Kelvin)
415.15
Boiling point (Celsius)
319.00
Boiling point (Kelvin)
592.15
General information
Molecular weight
201.22g/mol
Molar mass
201.2200g/mol
Density
1.2037g/cm3
Appearence

Carbaryl appears as a white crystalline solid. It is usually odorless or may have a faint characteristic odor. The crystals are often powdery in consistency.

Comment on solubility

Solubility of O-(2-naphthyl) N-methyl-N-(1-naphthyl)carbamothioate

The solubility of O-(2-naphthyl) N-methyl-N-(1-naphthyl)carbamothioate, a complex compound, can be influenced by several factors, making it an intriguing subject for study:

  • Polarity: Given the presence of the carbamothioate functional group, which contains sulfur, the polarity of this compound can impact its solubility in different solvents.
  • Solvent Interaction: This compound is likely to exhibit varying solubility in non-polar vs. polar solvents. For instance:
    • More soluble in non-polar solvents due to the naphthalene groups.
    • Less soluble in polar solvents due to potential hydrogen bonding interference.
  • Temperature: As with many organic compounds, an increase in temperature can generally improve solubility, allowing for better dissolution in the solvent.

Overall, while the exact solubility values would depend on specific experimental conditions, understanding these factors can aid researchers in predicting the behavior of O-(2-naphthyl) N-methyl-N-(1-naphthyl)carbamothioate in various chemical applications.

Interesting facts

Interesting Facts about O-(2-naphthyl) N-methyl-N-(1-naphthyl)carbamothioate

O-(2-naphthyl) N-methyl-N-(1-naphthyl)carbamothioate is a fascinating compound in the field of organic chemistry, particularly known for its diverse applications and intriguing structure. Here are some interesting aspects to consider:

  • Structural Complexity: This compound features a rich framework involving two naphthyl groups and a carbamothioate functional group, which contributes to its complex chemical behavior and unique reactivity.
  • Biological Activity: Compounds like this one often exhibit interesting biological activities. Many thioester derivatives are studied for their potential as agricultural pesticides or in pharmaceutical applications.
  • Research Applications: Its unique properties make it a subject of research in fields like materials science and medicinal chemistry, where understanding its interaction with biological systems can lead to the development of novel therapeutic agents.
  • Environmental Impact: The investigation of such compounds also extends to evaluating their environmental impact, particularly if they are used as pesticides, leading to considerations of their behavior in ecological systems.

A quote that encapsulates the importance of studying such compounds is: "Understanding the molecular underpinnings of chemical behavior can unveil solutions for productive applications and ecological safety."

In summary, O-(2-naphthyl) N-methyl-N-(1-naphthyl)carbamothioate is not only significant due to its intriguing structure but also because of its potential applications and the insights it can offer into both medicinal and environmental chemistry.

Synonyms
Naphtiomate-N
F83UDI8HTX
1049-15-6
Carbamothioic acid, methyl-1-naphthalenyl-, O-2-naphthalenyl ester
2-Naphthyl N-methyl-N-(1-naphthyl)thionocarbamate
1-Naphthalenecarbamic acid, N-methylthio-, O-2-naphthyl ester
AGN-PC-0JKBHK
UNII-F83UDI8HTX
o-(2-Naphthyl) methyl(1-naphthyl)thiocarbamate
o-(2-Naphthyl) N-methyl-N-(1-naphthyl)thiocarbamate
DTXSID30274535
ULKCSVORYFKCRE-UHFFFAOYSA-N
o-(2-Naphthyl) methyl(1-naphthyl)thiocarbamate #