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Carbaryl

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Identification
Molecular formula
C12H11NO2
CAS number
63-25-2
IUPAC name
[4-[formyl(methyl)amino]-3-methyl-phenyl] N-methylcarbamate
State
State
Carbaryl is a solid at room temperature, appearing as white crystals.
Melting point (Celsius)
142.00
Melting point (Kelvin)
415.15
Boiling point (Celsius)
290.00
Boiling point (Kelvin)
563.15
General information
Molecular weight
201.22g/mol
Molar mass
201.2210g/mol
Density
1.2300g/cm3
Appearence
Carbaryl typically appears as a white crystalline solid.
Comment on solubility

Solubility of [4-[formyl(methyl)amino]-3-methyl-phenyl] N-methylcarbamate

The solubility of a compound can often hold clues to its potential applications and behavior in various environments. When it comes to [4-[formyl(methyl)amino]-3-methyl-phenyl] N-methylcarbamate, several factors come into play:

  • Polar vs. Non-Polar: This compound has both polar and non-polar characteristics due to its functional groups, potentially affecting its solubility in different solvents.
  • Solvent Compatibility: The solubility may vary significantly between polar solvents (like water) and non-polar solvents (like hexane). It is expected to be more soluble in polar solvents due to the presence of the amine group which can engage in hydrogen bonding.
  • Temperature Effects: Generally, an increase in temperature can lead to increased solubility for many organic compounds. Therefore, evaluating [4-[formyl(methyl)amino]-3-methyl-phenyl] N-methylcarbamate under varying thermal conditions could yield interesting insights.
  • pH Sensitivity: Since the solubility of amine-containing compounds often is affected by pH, adjusting the pH of the solution may enhance its solubility characteristics.

In conclusion, while [4-[formyl(methyl)amino]-3-methyl-phenyl] N-methylcarbamate possesses intriguing solubility traits, further experimental data is necessary for a comprehensive understanding. It is always advisable to perform systematic solubility tests to ascertain its behavior in specific solvents and conditions.

Interesting facts

Interesting Facts About [4-[formyl(methyl)amino]-3-methyl-phenyl] N-methylcarbamate

This intriguing compound, often encountered in the realm of organic chemistry, presents a unique structural arrangement that fascinates chemists and researchers alike. Below, we explore some noteworthy aspects of this compound:

  • Complex Structure: The molecule contains multiple functional groups, including an amine and a carbamate, which contribute to its chemical reactivity and potential applications.
  • Potential Applications: Compounds with structures similar to this one are often investigated for their pharmacological properties, including potential as drug candidates due to their ability to interact with biological systems.
  • Synthesis Challenges: The synthesis of [4-[formyl(methyl)amino]-3-methyl-phenyl] N-methylcarbamate may require precise conditions and reagents, making it an interesting subject for synthetic chemists. The introduction of the formyl group adds a layer of complexity to the synthetic pathway.
  • Research Frontier: As with many organic compounds, ongoing research may reveal more about its properties and transformations, especially in the context of medicinal chemistry and materials science.

In the world of chemical compounds, understanding the subtleties of structure and function can pave the way for innovative discoveries and applications. This particular compound stands as a testament to the intricate relationship between molecular design and potential utility.

Synonyms
BRN 2740010
CARBAMIC ACID, METHYL-, ESTER with 4'-HYDROXY-N-METHYL-o-FORMOTOLUIDIDE
10233-98-4
Methylcarbamic acid ester with 4'-hydroxy-N-methyl-o-formotoluidide
DTXSID40144912
DTXCID7067403