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Carbaryl

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Identification
Molecular formula
C12H11NO2
CAS number
63-25-2
IUPAC name
1-naphthyl N-(hydroxymethyl)carbamate
State
State

At room temperature, carbaryl is in a solid state.

Melting point (Celsius)
142.00
Melting point (Kelvin)
415.15
Boiling point (Celsius)
350.00
Boiling point (Kelvin)
623.15
General information
Molecular weight
201.22g/mol
Molar mass
201.2210g/mol
Density
1.2300g/cm3
Appearence

Carbaryl appears as a white, crystalline solid with little to no odor.

Comment on solubility

Solubility of 1-naphthyl N-(hydroxymethyl)carbamate

The solubility of 1-naphthyl N-(hydroxymethyl)carbamate can be characterized in various solvent systems, which is crucial for understanding its chemical behavior in different environments. This compound exhibits interesting solubility properties that can be influenced by factors such as:

  • Polar and Nonpolar Solvents: Being a carbamate, it is expected to have varying solubility in polar solvents (such as water) compared to nonpolar solvents (such as hexane).
  • Temperature: Generally, an increase in temperature can enhance solubility for many organic compounds, including this carbamate.
  • pH Levels: The solubility may also be affected by the pH of the solution, as changes can alter the ionization state and, therefore, the solubility characteristics of the compound.

In summary, the solubility of 1-naphthyl N-(hydroxymethyl)carbamate is influenced by solvent type, temperature, and pH, which collectively affect its practical applications in chemical processes and formulations.

Interesting facts

Interesting Facts About 1-Naphthyl N-(hydroxymethyl)carbamate

1-Naphthyl N-(hydroxymethyl)carbamate is an intriguing compound that combines the structural features of naphthalene with a carbamate functional group. This unique combination results in a substance with both aromatic properties and significant biological activities.

Key Characteristics

  • Biological Relevance: Compounds similar to 1-naphthyl N-(hydroxymethyl)carbamate have been studied for their potential in pharmacology, especially in the development of pesticides and herbicides.
  • Mechanism of Action: The hydroxymethyl group may play a vital role in enhancing interactions with biological targets, making the compound a subject of interest in medicinal chemistry.
  • Aromatic Behavior: The naphthyl moiety contributes stability and unique electronic characteristics, crucial for its reactivity and interaction in various chemical processes.

Applications and Potential

This compound finds its potential applications in:

  1. Agricultural Chemistry: Serving as a potential agrochemical, it could provide an eco-friendly alternative to traditional pesticides.
  2. Pharmaceuticals: Research is ongoing to explore its effectiveness in drug formulation and design due to its structural elements.
  3. Materials Science: Its unique properties may lead to innovations in polymer chemistry and material engineering.

In conclusion, the fascinating structure and properties of 1-naphthyl N-(hydroxymethyl)carbamate open the door to exciting research avenues. As scientists continue to explore its potential, we may uncover new applications that can benefit multiple industries. The combination of chemistry with practical applications reiterates the importance of understanding such compounds in advancing science and technology.

Synonyms
1-Naphthyl (hydroxymethyl)carbamate
5266-96-6
Carbamic acid, hydroxymethyl-, 1-naphthalenyl ester
N-(Hydroxymethyl)carbaryl
(Hydroxymethyl)carbamic acid 1-naphthyl ester
BRN 2332151
AI3-28010
1-Naphthalenyl hydroxymethylcarbamate
CARBAMIC ACID, (HYDROXYMETHYL)-, 1-NAPHTHYL ESTER
DTXSID60274240
1-naphthyl N-hydroxymethyl-carbamate
NS00115912
Carbamic acid, N-(hydroxymethyl)-, 1-naphthalenyl ester