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Carbofuran

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Identification
Molecular formula
C12H15NO3
CAS number
1563-66-2
IUPAC name
chroman-8-yl N-methylcarbamate
State
State

At room temperature, Carbofuran is a solid.

Melting point (Celsius)
153.00
Melting point (Kelvin)
426.15
Boiling point (Celsius)
315.00
Boiling point (Kelvin)
588.15
General information
Molecular weight
221.26g/mol
Molar mass
221.2550g/mol
Density
1.1950g/cm3
Appearence

Carbofuran appears as a white crystalline solid.

Comment on solubility

Solubility of Chroman-8-yl N-methylcarbamate

The solubility of chroman-8-yl N-methylcarbamate can be quite intriguing due to its structural characteristics and functional groups. Understanding its solubility involves several factors:

  • Polar vs. Non-Polar: The presence of the carbamate group contributes to the overall polarity of the molecule, potentially enhancing solubility in polar solvents such as water.
  • Solvent Interaction: Chroman derivatives generally behave differently in various solvents. For example, they might show higher solubility in ethanol or dimethyl sulfoxide (DMSO) compared to water.
  • Temperature Influence: Like many organic compounds, the solubility of chroman-8-yl N-methylcarbamate can increase with temperature, affecting its dissolution characteristics in practical applications.
  • Structural Factors: The bulky chroman structure may hinder solubility in some organic solvents, making it necessary to explore solvent mixtures for optimal solubility.

In summary, while chroman-8-yl N-methylcarbamate may have moderate solubility in polar and some non-polar solvents, its behavior is ultimately dictated by the solvent environment. Exploring solubility profiles of this compound can reveal interesting insights into its chemical behavior in various applications.

Interesting facts

Interesting Facts about Chroman-8-yl N-methylcarbamate

Chroman-8-yl N-methylcarbamate is a fascinating compound that belongs to the broader class of carbamates, which are well-known for their diverse applications in various fields such as agriculture, pharmaceuticals, and industrial processes. Here are some intriguing aspects of this compound:

  • Structural Diversity: The structure of Chroman-8-yl N-methylcarbamate features a chroman moiety, which is a bicyclic structure containing oxygen. This unique configuration often leads to distinctive chemical properties.
  • Biological Significance: Compounds containing the carbamate functional group have been extensively studied for their biological activities. Some derivatives are known for their role as pesticides, while others have applications in medicinal chemistry.
  • Mechanism of Action: The N-methylcarbamate portion of the compound may interact with enzymes, particularly acetylcholinesterase, leading to interesting effects on neurotransmission. This raises potential implications for neuropharmacology.
  • Research Potential: Ongoing investigations into chroman-8-yl N-methylcarbamate and its derivatives may yield novel therapeutic agents. Scientists are particularly interested in exploring its potential as an anti-inflammatory or antioxidant agent.
  • Importance in Organic Synthesis: The functional groups present in this compound make it a valuable building block in organic synthesis, allowing chemists to develop more complex molecules efficiently.

The exploration of Chroman-8-yl N-methylcarbamate and its related derivatives offers a promising avenue for scientific discovery, bridging the gap between chemistry and potential real-world applications. As noted by chemists, "The beauty of organic molecules lies in their ability to create endless transformations and applications."

As research continues to unfold, the versatility of chroman-8-yl N-methylcarbamate may lead to surprising innovations across various fields.

Synonyms
Chromanyl-8 N-methylcarbamate
16146-52-4
2H-1-Benzopyran-8-ol, 3,4-dihydro-, methylcarbamate (9CI)
3,4-Dihydro-2H-1-benzopyran-8-ol methylcarbamate
CARBAMIC ACID, METHYL-, 8-CHROMANYL ESTER
2H-1-Benzopyran-8-ol, 3,4-dihydro-, methylcarbamate
DTXSID30167155
DTXCID0089646
3,4-dihydro-2H-chromen-8-yl N-methylcarbamate