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Carbaryl

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Identification
Molecular formula
C12H11NO2
CAS number
63-25-2
IUPAC name
(2-methoxy-4-prop-1-enyl-phenyl) N-methylcarbamate
State
State

At room temperature, Carbaryl is a solid. It is typically encountered as a powder or granular solid.

Melting point (Celsius)
142.00
Melting point (Kelvin)
415.15
Boiling point (Celsius)
260.00
Boiling point (Kelvin)
533.15
General information
Molecular weight
201.22g/mol
Molar mass
201.2200g/mol
Density
1.2300g/cm3
Appearence

Carbaryl is a white crystalline solid. It often appears as a solid powder that is colorless to white, and has a faint odor.

Comment on solubility

Solubility of (2-methoxy-4-prop-1-enyl-phenyl) N-methylcarbamate

The solubility of (2-methoxy-4-prop-1-enyl-phenyl) N-methylcarbamate can be influenced by a variety of factors, particularly its chemical structure and the nature of solvent interactions. Here are some key points regarding its solubility:

  • Polarity: This compound contains polar functional groups, which may enhance its solubility in polar solvents, such as water or alcohols.
  • Hydrophobic Character: The aromatic and aliphatic portions of the molecule may contribute to hydrophobic interactions, potentially reducing solubility in aqueous environments.
  • Temperature: Like many organic compounds, solubility can be temperature-dependent. Increasing the temperature may improve the solubility of (2-methoxy-4-prop-1-enyl-phenyl) N-methylcarbamate in suitable solvents.
  • Solvent Choice: It is essential to consider the solvent's compatibility. Organic solvents such as dimethyl sulfoxide (DMSO) or methanol may provide better solubility compared to water.

In summary, the solubility of (2-methoxy-4-prop-1-enyl-phenyl) N-methylcarbamate is a complex interplay of structural elements and solvent properties. As the saying goes, "like dissolves like," highlighting the importance of choosing the appropriate solvent to achieve optimal solubility.

Interesting facts

Interesting Facts about (2-methoxy-4-prop-1-enyl-phenyl) N-methylcarbamate

(2-methoxy-4-prop-1-enyl-phenyl) N-methylcarbamate is a compound that intrigues chemists and researchers alike due to its unique structural features and potential applications. Here are some fascinating aspects of this compound:

  • Acylurea Derivative: This compound belongs to the family of carbamates, which are known for their versatility in organic synthesis.
  • Biological Activity: Research indicates that similar structures can exhibit significant biological properties, making this compound a candidate for further exploration in medicinal chemistry.
  • Pesticidal Properties: Carbamate compounds are often studied for their effectiveness as pesticides due to their ability to inhibit cholinesterase, an important enzyme in nerve function.
  • Building Block for Synthesis: The unique arrangement of functional groups makes this compound an interesting building block for the synthesis of more complex organic molecules.
  • Environmental and Safety Considerations: As with many synthetic compounds, understanding the environmental impact and potential toxicity is crucial, emphasizing the importance of conducting thorough risk assessments.

In the realm of organic chemistry, the exploration of compounds like (2-methoxy-4-prop-1-enyl-phenyl) N-methylcarbamate not only enhances our understanding of chemical properties but also opens pathways for innovations in drug development and agrochemistry.

Since compounds in this class display a variety of reactivities, they invite further studies into their mechanisms of action and applications, making them a vibrant topic in contemporary chemical research.

Synonyms
(2-methoxy-4-prop-1-enylphenyl) N-methylcarbamate
NSC-191478
3YQ7B58CJH
Phenol, 2-methoxy-4-(1-propen-1-yl)-, 1-(N-methylcarbamate)