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Aldicarb

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Identification
Molecular formula
C7H14N2O2S
CAS number
116-06-3
IUPAC name
(2,2-dimethylchroman-8-yl) N-methylcarbamate
State
State

At room temperature, aldicarb is a solid. It is often found in granular formulations used for pesticide purposes.

Melting point (Celsius)
100.00
Melting point (Kelvin)
373.15
Boiling point (Celsius)
240.00
Boiling point (Kelvin)
513.15
General information
Molecular weight
190.24g/mol
Molar mass
190.2380g/mol
Density
1.1800g/cm3
Appearence

Aldicarb is a white crystalline compound. It is usually found in its pure form as a colorless crystalline solid.

Comment on solubility

Solubility of (2,2-dimethylchroman-8-yl) N-methylcarbamate

The solubility of (2,2-dimethylchroman-8-yl) N-methylcarbamate in various solvents can be influenced by several factors, including its molecular structure and polarity. Understanding its solubility is essential for applications in chemical synthesis and pharmaceutical formulations.

Key Considerations for Solubility:

  • Polarity: Compounds with higher polarity tend to dissolve better in polar solvents (like water), while non-polar solvents (such as hexane) work best for non-polar compounds.
  • Hydrogen Bonding: The presence of functional groups capable of hydrogen bonding can enhance solubility in certain solvents.
  • Molecular Weight: Generally, as the molecular weight of a compound increases, its solubility in a solvent may decrease.

For (2,2-dimethylchroman-8-yl) N-methylcarbamate, interactions with solvents can vary significantly:

  1. In polar solvents, the solubility may be moderate due to potential hydrogen bonding.
  2. In organic solvents, it may exhibit good solubility thanks to its relatively non-polar character.

As with many organic compounds, the *specific solubility behavior* will depend on the experimental conditions, including temperature and the medium used. Knowledge of solubility plays a crucial role in determining its application in various chemical processes.

Interesting facts

Interesting Facts about (2,2-dimethylchroman-8-yl) N-methylcarbamate

(2,2-dimethylchroman-8-yl) N-methylcarbamate is a fascinating compound that merges the worlds of organic chemistry and medicinal applications. This compound is in the class of carbamates, which are known for their diverse biological activities.

Key Highlights

  • Biological Relevance: Carbamates exhibit a wide range of pharmacological effects, making them crucial in drug development. They can act as enzyme inhibitors and have applications in treating various diseases.
  • Structure and Function: The unique chroman ring structure contributes to the compound's properties. The dimethyl substitution on the chroman enhances its lipophilicity, potentially impacting the bioavailability and interaction with biological targets.
  • Synthesis: The synthesis of this compound typically involves multistep organic reactions that may include nucleophilic substitutions and coupling reactions, showcasing the versatility of organic synthesis techniques.
  • Environmental Impact: As with many carbamates, the potential for environmental persistence and toxicity is an aspect that researchers continuously study, leading to the development of safer alternatives.

Research into compounds like (2,2-dimethylchroman-8-yl) N-methylcarbamate opens avenues for new therapeutic agents and enhances our understanding of complex organic molecules. As the field of medicinal chemistry evolves, this compound exemplifies the synergy of chemistry and pharmacology, making it an exciting topic for further investigation.

Synonyms
Niagara 11637
Niagara 10856
2,2-Dimethylchromanyl-8 N-methylcarbamate
NIA-11637
FMC 11637
ENT 27,385
CARBAMIC ACID, METHYL-, 2,2-DIMETHYL-8-CHROMANYL ESTER
AI3-27385
IYD478G664
UNII-IYD478G664
3,4-Dihydro-2,2-dimethyl-2H-1-benzopyran-8-yl methylcarbamate
DTXSID90167156
2H-1-Benzopyran-8-ol, 2,3-dihydro-2,2-dimethyl-, methylcarbamate
8-CHROMANOL, 2,2-DIMETHYL-, METHYLCARBAMATE
2H-1-BENZOPYRAN-8-OL, 3,4-DIHYDRO-2,2-DIMETHYL-, METHYLCARBAMATE
2H-1-BENZOPYRAN-8-OL, 3,4-DIHYDRO-2,2-DIMETHYL-, 8-(N-METHYLCARBAMATE)
DTXCID5089647
16146-62-6