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Carbaryl

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Identification
Molecular formula
C12H11NO2
CAS number
63-25-2
IUPAC name
(2-allyloxyphenyl) N-methylcarbamate
State
State

At room temperature, carbaryl is typically found in a solid state. It is stable under normal conditions but can degrade in the presence of moisture, light, or strong acids and bases.

Melting point (Celsius)
142.00
Melting point (Kelvin)
415.15
Boiling point (Celsius)
295.00
Boiling point (Kelvin)
568.15
General information
Molecular weight
201.22g/mol
Molar mass
201.2210g/mol
Density
1.2300g/cm3
Appearence

Carbaryl is typically present as a white crystalline solid. It is odorless and has a slightly sweet taste. It is usually manufactured in powder or granular form for its use as a pesticide.

Comment on solubility

Solubility of (2-allyloxyphenyl) N-methylcarbamate

The solubility of (2-allyloxyphenyl) N-methylcarbamate can be influenced by several factors, including its molecular structure and the nature of the solvent. This compound displays qualities that may allow for variable solubility profiles:

  • Polar vs. Nonpolar Solvents: As a carbamate, (2-allyloxyphenyl) N-methylcarbamate may exhibit different solubility characteristics in polar versus nonpolar solvents. Generally, compounds that have strong polar functional groups are more soluble in polar solvents.
  • Temperature Effects: Like many organic compounds, its solubility may increase with an increase in temperature, leading to higher dissolution rates.
  • pH Sensitivity: The solubility could be influenced by the pH of the solvent, especially in the presence of acidic or basic conditions which can affect ionization.
  • Hydrogen Bonding: The presence of hydrogen bond donors or acceptors in the solvent can enhance interactions with the compound, affecting its solubility positively.

In summary, while specific solubility data may not be extensively documented for (2-allyloxyphenyl) N-methylcarbamate, understanding the relationship between its chemical structure and the properties of the solvent is crucial. Remember, "the solubility of a substance is often the key to its potential applications!"

Interesting facts

Interesting Facts about (2-allyloxyphenyl) N-methylcarbamate

(2-allyloxyphenyl) N-methylcarbamate is a fascinating compound that showcases the diversity and utility of carbamates in chemistry. Here are some interesting points to consider:

  • Carbamate Class: This compound belongs to the carbamate family, which are esters of carbamic acid. The presence of the carbamate functional group is significant as it often relates to biological activity and pharmaceutical applications.
  • Potential Applications: (2-allyloxyphenyl) N-methylcarbamate may have potential in agricultural chemistry as a pesticide or herbicide. The unique structure might contribute to its ability to interact with biological systems, impacting pests specifically.
  • Synthesis: The synthesis of carbamates is typically achieved through the reaction of isocyanates with alcohols or amines. Understanding the synthetic pathways is essential for developing derivatives with enhanced properties.
  • Biological Relevance: Many carbamates have been studied for their inhibitory effects on acetylcholinesterase, making them relevant in the context of neurobiology and toxicology. The activity profiles of compounds like (2-allyloxyphenyl) N-methylcarbamate might contribute to broader research in these areas.
  • Research Trends: Current research trends involve examining the medicinal properties of carbamates. (2-allyloxyphenyl) N-methylcarbamate could be a candidate for further investigation to evaluate its therapeutic potential.

As chemists explore the attributes of compounds like (2-allyloxyphenyl) N-methylcarbamate, the implications for various fields, such as pharmacology, agriculture, and material science, become increasingly significant. Each molecule tells a story, unlocking new possibilities in chemical research.

Synonyms
Hercules 9,485
4062-99-1
CARBAMIC ACID, N-METHYL-, o-(ALLYLOXY)PHENYL ESTER
2-(2-Propenyloxy)phenol methylcarbamate
BRN 1968999
Hercules 9485
AI3-25912
2-(Allyloxy)phenyl methylcarbamate
DTXSID00193628
Carbamic acid, methyl-, o-(allyloxy)phenyl ester
Phenol, o-(allyloxy)-, methylcarbamate
DTXCID40116119
rrcxoibmskrasz-uhfffaoysa-n
o-(Allyloxy)phenyl methylcarbamate
He 9485
HRS 9485
Phenol, 2-(2-propenyloxy)-, methylcarbamate
SCHEMBL8754763