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Propoxur

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Identification
Molecular formula
C11H15NO3
CAS number
114-26-1
IUPAC name
(2-ethyl-2-methyl-1,3-benzodioxol-4-yl) N-methylcarbamate
State
State

At room temperature, propoxur is typically found in a solid state.

Melting point (Celsius)
91.50
Melting point (Kelvin)
364.65
Boiling point (Celsius)
360.00
Boiling point (Kelvin)
633.15
General information
Molecular weight
209.25g/mol
Molar mass
209.2260g/mol
Density
1.1600g/cm3
Appearence

Propoxur is a white to off-white crystalline solid. It may also be found in powder form and is odorless or has a faint characteristic odor.

Comment on solubility

Solubility of (2-ethyl-2-methyl-1,3-benzodioxol-4-yl) N-methylcarbamate

The solubility of (2-ethyl-2-methyl-1,3-benzodioxol-4-yl) N-methylcarbamate can be influenced by various factors. Here are some key points to consider:

  • Polarity: The presence of both hydrophobic and hydrophilic regions in the molecule suggests that it may have varied solubility in different solvents.
  • Solvent Interaction: It is likely to exhibit better solubility in organic solvents like ethanol and acetone, rather than in polar solvents like water.
  • Functional Groups: The carbamate moiety typically enhances the solubility of compounds in polar solvents, but the overall structure might lead to limited solubility in water.
  • Temperature Dependence: Like many organic compounds, its solubility may increase with temperature, making it easier to dissolve at elevated temperatures.

In summary, the solubility of (2-ethyl-2-methyl-1,3-benzodioxol-4-yl) N-methylcarbamate is context-dependent, and examining its behavior in various solvents can provide better insights into its applications and usage.

Interesting facts

Interesting Facts about (2-ethyl-2-methyl-1,3-benzodioxol-4-yl) N-methylcarbamate

(2-ethyl-2-methyl-1,3-benzodioxol-4-yl) N-methylcarbamate is a fascinating compound belonging to the broader class of carbamates. Here are some intriguing details that make this compound noteworthy:

  • Chemical Structure: This compound showcases a unique combination of both a carbamate functional group and a complex fused benzodioxole structure. This architectural design often leads to enhanced bioactivity and interactions with biological targets.
  • Biological Activity: Carbamates, in general, have been researched for their potential in medicinal chemistry. They can possess various biological activities, which may include enzyme inhibition or interaction with neurotransmitter systems.
  • Applications: Compounds similar to (2-ethyl-2-methyl-1,3-benzodioxol-4-yl) N-methylcarbamate have been investigated for uses in agriculture, particularly as insecticides or pesticides, owing to their ability to affect the nervous systems of pests.
  • Research Interest: Due to its complex structure, this compound may be of interest in the field of synthetic organic chemistry, facilitating the development of new synthetic methods or the exploration of novel reactions that could yield variations in biological efficacy.
  • Quote from the Field: "The ability to modify structure and predict the resulting biological behavior is what makes carbamate chemistry so compelling," says a chemist studying these compounds.

Overall, the study of (2-ethyl-2-methyl-1,3-benzodioxol-4-yl) N-methylcarbamate not only emphasizes the intricate relationship between chemical structure and function but also highlights the potential avenues for practical applications in both pharmacology and agrochemical industries.

Synonyms
22781-24-4
2-Ethyl-2-methyl-1,3-benzodioxol-4-ol methylcarbamate
DTXSID00945462
2-Ethyl-2-methyl-2H-1,3-benzodioxol-4-yl hydrogen methylcarbonimidate
BRN 1318490
1,3-BENZODIOXOL-4-OL, 2-ETHYL-2-METHYL-, METHYLCARBAMATE
RefChem:1063026
DTXCID601373777