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Phenoxicarb

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Identification
Molecular formula
C12H13NO4
CAS number
79127-80-3
IUPAC name
2,3-dihydro-1,4-benzodioxin-5-yl N-methylcarbamate
State
State

Phenoxicarb is in a solid state at room temperature.

Melting point (Celsius)
41.00
Melting point (Kelvin)
314.00
Boiling point (Celsius)
434.50
Boiling point (Kelvin)
707.70
General information
Molecular weight
221.24g/mol
Molar mass
221.2480g/mol
Density
1.2740g/cm3
Appearence

Phenoxicarb is typically a colorless to pale yellow crystalline solid.

Comment on solubility

Solubility of 2,3-dihydro-1,4-benzodioxin-5-yl N-methylcarbamate

The solubility of 2,3-dihydro-1,4-benzodioxin-5-yl N-methylcarbamate can be influenced by several factors. Here are some important points to consider:

  • Polar vs. Nonpolar Solvents: This compound tends to have moderate solubility in polar solvents such as water and alcohols, which is characteristic of most carbamate derivatives.
  • Temperature Influence: Solubility can increase with temperature, making higher temperatures favorable for dissolution in solution.
  • pH Levels: The solubility may vary significantly with changes in pH, as the protonation state can affect its interactions with solvent molecules.
  • Structural Factors: The benzodioxin moiety contributes to its overall solubility profile due to steric hindrance and electronic effects that influence how this compound interacts with solvents.

Overall, understanding the solubility of 2,3-dihydro-1,4-benzodioxin-5-yl N-methylcarbamate is crucial for its applications and can be summarized as follows:

  1. The compound is likely to be more soluble in solvents that facilitate hydrogen bonding.
  2. Practical applications may be affected by its solubility characteristics, making it essential to consider when formulating with this compound.
  3. Environmental factors and conditions will play a role in how this compound behaves in different environments.

In conclusion, the solubility of 2,3-dihydro-1,4-benzodioxin-5-yl N-methylcarbamate presents interesting considerations for both research and application in various fields.

Interesting facts

Interesting Facts about 2,3-Dihydro-1,4-benzodioxin-5-yl N-methylcarbamate

This intriguing compound, known for its unique structural characteristics, holds significant potential in various fields of chemistry and pharmaceuticals. Here are some fascinating insights:

  • Structure and Stability: The compound features a stable benzodioxin moiety, which is known for its aromaticity and robustness, contributing to the overall stability of the molecule.
  • Biological Activity: Compounds similar to this one have been studied for their potential biological activity, including insecticidal properties. This makes them of particular interest in agricultural chemistry.
  • Versatile Applications: The presence of the N-methylcarbamate group suggests potential use as a pesticide or herbicide, as carbamates are often effective in targeting specific pests with minimal environmental impact.
  • Synthetic Routes: The synthesis of this compound can involve various chemical reactions, including nucleophilic substitutions and cyclization processes, which are essential topics in organic chemistry.
  • Environmental Considerations: As with all chemical compounds, understanding the environmental fate and degradation of this compound is crucial, especially given its potential use in agricultural settings.

As noted by researchers in the field, "The integration of different functional groups within such compounds often leads to a treasure trove of biological and chemical interactions, waiting to be explored." This is a reminder of the vast possibilities that chemistry brings to our world.

In summary, 2,3-dihydro-1,4-benzodioxin-5-yl N-methylcarbamate exemplifies the unique fusion of complex structure with practical application, making it a compound worth studying further in the realms of chemistry and environmental science.

Synonyms
Stauffer R-11163
13792-21-7
ENT 27,362
CARBAMIC ACID, METHYL-, 1,4-BENZODIOXAN-5-YL ESTER
NSC 67279
1,4-Benzodioxan-5-yl methylcarbamate
BRN 1315337
R-11163
AI3-27362
1,4-Benzodioxin-5-ol, 2,3-dihydro-, methylcarbamate
DTXSID00160395
DTXCID8082886
WY32GJA26G
2,3-Dihydro-1,4-benzodioxin-8-yl N-methylcarbamate
1,4-Benzodioxan-5-ol, methylcarbamate
1,4-Benzodioxin-5-ol, 2,3-dihydro-, 5-(N-methylcarbamate)