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Aldicarb

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Identification
Molecular formula
C7H14N2O2S
CAS number
116-06-3
IUPAC name
[(1,2-dimethyl-2-nitro-propylidene)amino] N-methylcarbamate
State
State

Aldicarb is typically in a solid state at room temperature.

Melting point (Celsius)
100.50
Melting point (Kelvin)
373.65
Boiling point (Celsius)
306.00
Boiling point (Kelvin)
579.15
General information
Molecular weight
190.23g/mol
Molar mass
190.2290g/mol
Density
1.1940g/cm3
Appearence

Aldicarb appears as a colorless crystalline solid. It has no distinct smell, but it is known for its high toxicity and effectiveness as a pesticide.

Comment on solubility

Solubility of [(1,2-dimethyl-2-nitro-propylidene)amino] N-methylcarbamate

The solubility of [(1,2-dimethyl-2-nitro-propylidene)amino] N-methylcarbamate can be influenced by various factors including temperature, solvent choice, and molecular interactions. Here are some key points to consider:

  • Polar vs. Nonpolar Solvents: The polarity of the solvent plays a crucial role in determining the solubility of this compound. Compounds with polar functional groups may have enhanced solubility in polar solvents like water and alcohols.
  • Temperature Effects: As temperature increases, solubility typically increases for many solids. However, this is not a universal rule and may vary based on specific interactions within the compound.
  • pH Dependence: Since this compound contains an amine group, the pH of the medium can significantly affect its solubility. In more acidic conditions, the amine may become protonated, affecting interactions with the solvent.
  • Molecular Interactions: The presence of functional groups can lead to hydrogen bonding, dipole-dipole interactions, or van der Waals forces, which can enhance or impede solubility. For example, the nitro group may introduce some solubility in certain solvents that can stabilize these interactions.

In practice, one might say, "Like dissolves like." Hence, understanding the chemical nature of [(1,2-dimethyl-2-nitro-propylidene)amino] N-methylcarbamate is indispensable for predicting its solubility in various solvents.

Overall, while specific solubility data may not be readily available, careful consideration of these factors will provide a clearer picture of how this compound interacts with different environments.

Interesting facts

Interesting Facts about [(1,2-dimethyl-2-nitro-propylidene)amino] N-methylcarbamate

[(1,2-dimethyl-2-nitro-propylidene)amino] N-methylcarbamate represents a fascinating compound that belongs to the class of carbamates, known for their diverse applications in agriculture and pharmaceuticals.

Key Features:

  • Structural Uniqueness: This compound features a complex arrangement of functional groups that contribute to its distinct chemical properties.
  • Biologically Active: As a member of the carbamate family, it often interacts with biological systems, potentially acting as a selective inhibitor of certain enzymes.
  • Safety Measures: Due to its nitro group, it is important for chemists to handle it with care, as nitro compounds can be sensitive under certain conditions.

This compound exemplifies the rich intersection of organic synthesis and medicinal chemistry. As highlighted by one renowned chemist, "Innovation often stems from the exploration of complex molecules, revealing possibilities that transform industries." Whether you are studying its synthesis or exploring its reactivity, the compound provides ample opportunities for research and discovery.

Applications:

  • Agricultural Uses: It could potentially serve as a precursor in the development of pesticides or herbicides, helping to protect crops.
  • Pharmaceutical Research: Further studies on this compound could unveil new therapeutic pathways, enhancing our understanding of disorders that are susceptible to biochemical modulation.

In sum, [(1,2-dimethyl-2-nitro-propylidene)amino] N-methylcarbamate is not just a compound of interest due to its molecular structure, but also due to the potential it holds for future innovations in chemistry and industry.

Synonyms
DB-324592
3-METHYL -3-NITRO-2-BUTANONE O-(METHYLCARBAMOYL )OXIME