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Carbofuran

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Identification
Molecular formula
C12H15N2O3
CAS number
1563-66-2
IUPAC name
(2-methyl-8-quinolyl) N-methylcarbamate
State
State

Carbofuran is a solid at room temperature.

Melting point (Celsius)
153.00
Melting point (Kelvin)
426.15
Boiling point (Celsius)
275.00
Boiling point (Kelvin)
548.15
General information
Molecular weight
221.26g/mol
Molar mass
221.2570g/mol
Density
1.1800g/cm3
Appearence

Carbofuran appears as a white crystalline solid. It has a slightly musty odor.

Comment on solubility

Solubility of (2-methyl-8-quinolyl) N-methylcarbamate

(2-methyl-8-quinolyl) N-methylcarbamate, a compound known for its intriguing structure, exhibits notable solubility characteristics. Its solubility largely depends on the solvent employed, which can lead to varied outcomes. Here are some key points to consider:

  • Polar Solvents: Generally, (2-methyl-8-quinolyl) N-methylcarbamate shows improved solubility in polar solvents such as water and methanol due to its functional groups which can engage in hydrogen bonding.
  • Non-Polar Solvents: In contrast, its solubility in non-polar solvents like hexane is significantly lower. The hydrophobic regions of the compound limit its interaction with such solvents.
  • Temperature Effects: As with many chemical compounds, increasing the temperature can enhance solubility. For instance, a warm methanol solution may allow more of the compound to dissolve compared to a cold one.
  • pH Dependence: The solubility can also be influenced by the pH of the solvent, as ionization of the amine or carbamate groups can affect overall solubility.

As is often the case with organic compounds, the solubility of (2-methyl-8-quinolyl) N-methylcarbamate is multifaceted, highlighting the importance of selecting appropriate solvents for dissolution and application. Thus, careful consideration of environmental factors will yield the best results for this compound.

Interesting facts

Interesting Facts about (2-methyl-8-quinolyl) N-methylcarbamate

The compound known as (2-methyl-8-quinolyl) N-methylcarbamate is a fascinating member of the carbamate family, featuring a unique structure that combines the properties of both quinoline and carbamate functional groups. Here are some captivating aspects of this compound:

  • Biological Activity: The incorporation of the quinoline moiety is significant, as many quinoline derivatives are known for their biological activities, including antimicrobial and antimalarial properties. This renders (2-methyl-8-quinolyl) N-methylcarbamate a potential candidate for medication development.
  • Pesticidal Uses: Many carbamates are utilized in agricultural applications as pesticides. It’s intriguing to explore whether (2-methyl-8-quinolyl) N-methylcarbamate exhibits similar characteristics, which could enhance pest management strategies.
  • Synthesis: The methods of synthesizing this compound can involve the reaction of 2-methyl-8-quinoline with N-methylcarbamoyl chloride. Studying synthesis techniques helps chemists optimize yields and improve the efficiency of producing such compounds.
  • Research Potential: Given its structural complexity, this compound opens avenues for research in areas like drug design and environmental science. Scientists might investigate its effects on different biological systems or its interactions with various enzymes.
  • Analytical Techniques: Characterizing (2-methyl-8-quinolyl) N-methylcarbamate might involve techniques such as NMR, mass spectrometry, or HPLC. These methods are crucial for confirming the identity and purity of the compound in research settings.

In summary, (2-methyl-8-quinolyl) N-methylcarbamate exemplifies how a single compound can encapsulate a wealth of scientific intrigue, from its synthesis to its potential applications. As researchers continue to explore its properties, there is a strong possibility that this compound may play a significant role in the fields of medicine and environmental chemistry.

Synonyms
Giegy GS-13798
Ciba C-7824
14628-06-9
ENT 27,407
NSC 190997
8-(Methyl-quinolyl)-N-methyl carbamate
BRN 1532234
CARBAMIC ACID, METHYL-, (2-METHYL-8-QUINOLYL) ESTER
8-Quinolinol, 2-methyl-, methylcarbamate (ester)
AI3-27407
GS-13,798
C 7824
8-Quinolinol, 2-methyl-, methylcarbamate
DTXSID90163335
DTXCID0085826
MCMO
SCHEMBL4456603
SCHEMBL29421076