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Fenobucarb

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Identification
Molecular formula
C12H16ClNO2
CAS number
3766-81-2
IUPAC name
(2-chloro-6-isopropyl-3-methyl-phenyl) N-methylcarbamate
State
State

At room temperature, fenobucarb is in a liquid state, which allows it to be used conveniently in various agricultural applications, involving spraying or dilution processes.

Melting point (Celsius)
3.00
Melting point (Kelvin)
276.00
Boiling point (Celsius)
383.00
Boiling point (Kelvin)
656.00
General information
Molecular weight
207.69g/mol
Molar mass
207.6890g/mol
Density
1.1000g/cm3
Appearence

Fenobucarb appears as a colorless to light brown liquid. Depending on its purity, it may exhibit a slight aromatic odor. It is typically used in agricultural settings where its appearance is maintained in a stable, liquid form to facilitate its application.

Comment on solubility

Solubility of (2-chloro-6-isopropyl-3-methyl-phenyl) N-methylcarbamate

The solubility of (2-chloro-6-isopropyl-3-methyl-phenyl) N-methylcarbamate is influenced by its chemical structure, which presents both hydrophobic and polar characteristics. Generally, the solubility of this compound can be assessed through the following key factors:

  • Hydrophobic Interactions: The presence of the isopropyl and chlorinated groups contributes to the hydrophobic nature of the compound, which can lead to lower solubility in polar solvents.
  • Polar Characteristics: The N-methylcarbamate group has polar properties, making the compound potentially soluble in polar organic solvents such as methanol and ethanol.
  • Temperature Effects: Solubility is also temperature-dependent; as temperature increases, solubility in solvents may improve for many compounds.

In practical terms, the solubility of (2-chloro-6-isopropyl-3-methyl-phenyl) N-methylcarbamate is expected to be:

  1. Moderate in organic solvents, particularly those with polar characteristics.
  2. Limited in water, due to its hydrophobic groups.

As a rule of thumb, compounds with both hydrophobic and polar features may exhibit solubility in mixed solvent systems, where the balance between these characteristics can enhance dissolution. Analyzing specific solvent interactions would provide a clearer understanding of its solubility profile.

Interesting facts

Interesting Facts about (2-chloro-6-isopropyl-3-methyl-phenyl) N-methylcarbamate

(2-chloro-6-isopropyl-3-methyl-phenyl) N-methylcarbamate is a fascinating compound with a broad range of applications, particularly in the field of agriculture and pest control. This compound belongs to the class of carbamates, which are often utilized for their efficacy as pesticides, particularly insecticides and herbicides.

Key Characteristics

  • Mechanism of Action: Carbamates work by inhibiting the enzyme acetylcholinesterase, leading to an accumulation of acetylcholine in the synaptic cleft, which can be detrimental to pest populations.
  • Targeted Use: This compound can be specifically used against a variety of agricultural pests, making it a valuable tool for farmers aiming to protect their crops.
  • Environmental Considerations: While effective, the environmental impact of carbamates is a key consideration, as they can affect non-target species, including beneficial insects and aquatic life.

Exciting Applications

The versatility of (2-chloro-6-isopropyl-3-methyl-phenyl) N-methylcarbamate extends beyond agriculture:

  • Pesticide Development: Researchers are continually exploring derivatives and analogs of this compound to enhance efficacy and reduce environmental risk.
  • Biochemistry Studies: Its relevance in studying synaptic transmission and enzyme inhibition provides insights into neurological responses.
  • Safety Profiles: It is critical to assess the toxicity and safety mechanisms of carbamates, which drives research in toxicology and pharmacology.

In summary, (2-chloro-6-isopropyl-3-methyl-phenyl) N-methylcarbamate is not just a chemical compound; it is a crucial player in the intersection of agricultural science, environmental stewardship, and biochemistry. As researchers continue to explore its full potential and implications, it remains a significant topic of interest within the scientific community. As the famous quote goes, "Chemistry is the language of nature," and compounds like this one help us decode that language in exciting ways!

Synonyms
CARBAMIC ACID, METHYL-, 6-CHLOROTHYMYL ESTER
17578-41-5
6-Chlorothymyl methylcarbamate
N-Methylcarbamate of 6-chlorothymol
BRN 2271446
DTXSID30170023
2-chloro-6-isopropyl-3-methylphenyl methylcarbamate
2655-03-0