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Carbaryl

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Identification
Molecular formula
C12H11NO2
CAS number
63-25-2
IUPAC name
(1,3,3-trimethylnorbornan-2-yl) N-methylcarbamate
State
State
Solid at room temperature. Typically available as a powder or crystalline solid.
Melting point (Celsius)
142.50
Melting point (Kelvin)
415.65
Boiling point (Celsius)
302.00
Boiling point (Kelvin)
575.15
General information
Molecular weight
201.22g/mol
Molar mass
201.2210g/mol
Density
1.2510g/cm3
Appearence

Carbaryl is a white crystalline solid. It is often sold in a powdered form or as a liquid suspension.

Comment on solubility

Solubility of (1,3,3-trimethylnorbornan-2-yl) N-methylcarbamate

The solubility of (1,3,3-trimethylnorbornan-2-yl) N-methylcarbamate can be influenced by various factors, making it an intriguing compound to study. Here are some key points regarding its solubility:

  • Polarity: The solubility of this compound may primarily depend on its polar and nonpolar characteristics. As a carbamate, it can exhibit some polar behavior due to the amine and carbonyl groups present.
  • Solvent Interaction: It is likely to show adequate solubility in polar organic solvents such as methanol or ethanol, while possibly having limited solubility in nonpolar solvents like hexane.
  • Temperature Dependence: As with many organic compounds, solubility can increase with temperature. Higher temperatures usually enhance solubility, allowing for better mixing and dissolution in suitable solvents.
  • Functional Groups: The presence of functional groups such as the N-methylcarbamate can improve interactions with solvent molecules. Specifically, hydrogen bonding may facilitate the solubility in aqueous or polar environments.

Overall, to determine the exact solubility of (1,3,3-trimethylnorbornan-2-yl) N-methylcarbamate, empirical testing in various solvents is recommended, as theoretical predictions can sometimes diverge from experimental observations.

Interesting facts

Interesting Facts About (1,3,3-trimethylnorbornan-2-yl) N-methylcarbamate

(1,3,3-trimethylnorbornan-2-yl) N-methylcarbamate is a fascinating compound that falls within the class of carbamates, which are known for their versatility and wide-ranging applications. This particular structure is characterized by its complex bicyclic carbon framework, depicting a unique blend of rigidity and reactivity.

Key Features of the Compound:

  • Carbamate Functionality: As a member of the carbamate family, this compound showcases the ability to act as a nutrient and environmental stress mitigator in agricultural applications.
  • Synthetic Applications: It serves as an important intermediate in the synthesis of various pharmaceuticals, illustrating its significance in medicinal chemistry.
  • Biological Activity: Due to its structural features, it has been studied for potential biological activities, making it a point of interest in drug design and discovery.

This compound's intriguing structure leads to diverse reactivity patterns, marking its importance in research. As chemists explore new uses or modifications of this compound, they often remark on its implications in enhancing the efficiency of chemical reactions. As one prominent chemist once said, "The chemistry of carbamates offers not just complexity, but an opportunity to innovate."

Research on (1,3,3-trimethylnorbornan-2-yl) N-methylcarbamate continues to evolve, revealing potential contributions to sustainable practices in agriculture and environmentally friendly pest control methods. Its unique structural attributes open the door to numerous possibilities in both academic and industrial chemistry, making it an area ripe for exploration.

Synonyms
alpha-Fenchyl alcohol methylcarbamate
1,3,3-Trimethyl-2-norbornyl methylcarbamate
N-Methylcarbamate of alpha-fenchyl alcohol
17578-44-8
CARBAMIC ACID, METHYL-, 1,3,3-TRIMETHYL-2-NORBORNYL ESTER
DTXSID30938701
1,3,3-Trimethylbicyclo[2.2.1]heptan-2-yl hydrogen methylcarbonimidate