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Aldicarb

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Identification
Molecular formula
C7H14ClN3O2
CAS number
116-06-3
IUPAC name
[[(3S,6S)-3-chloro-6-cyano-norbornan-2-ylidene]amino] N-methylcarbamate
State
State

At room temperature, Aldicarb is in a solid state, and it is commonly encountered as a crystalline powder.

Melting point (Celsius)
100.00
Melting point (Kelvin)
373.15
Boiling point (Celsius)
280.00
Boiling point (Kelvin)
553.15
General information
Molecular weight
190.27g/mol
Molar mass
190.2730g/mol
Density
1.1950g/cm3
Appearence

Aldicarb typically appears as a white crystalline solid.

Comment on solubility

Solubility of [[(3S,6S)-3-chloro-6-cyano-norbornan-2-ylidene]amino] N-methylcarbamate

The solubility of the compound [[ (3S,6S)-3-chloro-6-cyano-norbornan-2-ylidene]amino] N-methylcarbamate is influenced by its unique structural features. Understanding solubility can be essential for applications in pharmaceuticals, agrochemicals, and materials science. Here are key points regarding its solubility:

  • Polarity: The presence of both a cyano group (-C≡N) and a carbamate functional group may enhance the compound’s interaction with polar solvents, influencing solubility.
  • Hydrogen Bonding: The amino group can participate in hydrogen bonding, which can further increase solubility in polar solvents.
  • Solvent Dependency: The compound is likely to exhibit different solubility profiles in various solvents such as water, ethanol, or organic solvents like acetone.
  • Temperature Effects: Solubility may be temperature-dependent; generally, increased temperature can enhance solubility for many compounds.
  • pH Sensitivity: The charge and state of ionization of the amino and carbamate groups may shift with pH changes, affecting solubility.

In summary, while [[ (3S,6S)-3-chloro-6-cyano-norbornan-2-ylidene]amino] N-methylcarbamate is expected to be soluble in polar solvents due to its functional groups, specific solubility characteristics should be examined experimentally to fully understand its behavior in different environments. Understanding these aspects can significantly aid in the practical applications of this compound.

Interesting facts

Interesting Facts about [(3S,6S)-3-chloro-6-cyano-norbornan-2-ylidene]amino N-methylcarbamate

This compound, a derivative of norbornane, holds significant interest due to its unique structural characteristics and potential applications in various fields. Let's delve into some intriguing aspects:

  • Stereochemistry: The compound has a well-defined stereochemistry, indicated by the (3S,6S) configuration. This is critical in understanding its reactivity and interactions with biological systems.
  • Functional Groups: With a chlorinated and cyano functional group, the compound showcases reactivity that can be leveraged in organic synthesis, particularly in the formation of complex molecules.
  • Potential Applications: Compounds like this have potential uses in agrochemicals, specifically as pesticides or herbicides, due to their ability to interact with biological pathways. Their ability to influence plant or insect physiology makes them invaluable in agricultural chemistry.
  • Research Significance: The structural features of this compound are of interest to researchers aiming to design new substances that exhibit selective activity against pests while minimizing environmental impact.
  • Mechanism of Action: Understanding how the presence of the cyano and chloro groups affects the pharmacodynamics of the molecule could pave the way for new classes of agrochemicals.

As chemistry students and scientists explore compounds like [(3S,6S)-3-chloro-6-cyano-norbornan-2-ylidene]amino N-methylcarbamate, they are reminded that the interplay of structure and reactivity can lead to innovative solutions in both scientific and practical applications.