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Chlorphenesin carbamate

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Identification
Molecular formula
C10H12ClNO3
CAS number
80-29-1
IUPAC name
[2-(2-chlorophenyl)-1-methyl-ethyl] carbamate
State
State

At room temperature, chlorphenesin carbamate is in a solid state, typically appearing as a powder.

Melting point (Celsius)
77.00
Melting point (Kelvin)
350.00
Boiling point (Celsius)
250.00
Boiling point (Kelvin)
523.00
General information
Molecular weight
213.67g/mol
Molar mass
213.6680g/mol
Density
1.2800g/cm3
Appearence

Chlorphenesin carbamate is typically a white crystalline solid. It is often found as a powder and may have a slight characteristic odor.

Comment on solubility

Solubility of [2-(2-chlorophenyl)-1-methyl-ethyl] carbamate

The solubility of [2-(2-chlorophenyl)-1-methyl-ethyl] carbamate can be influenced by several factors, reflecting its chemical structure and interactions in various solvents. Understanding these can help predict its behavior in different environments. Here are some key points to consider:

  • Polarity: Due to the presence of both a carbamate group and a chlorophenyl ring, the compound exhibits a degree of polarity which can enhance solubility in polar solvents.
  • Solvent Affinity: It is likely to be more soluble in organic solvents such as ether or acetone, while showing limited solubility in water.
  • Temperature Influence: As with many organic compounds, solubility may increase with temperature, suggesting that heating could improve its dissolution in suitable solvents.
  • pH Dependence: The solubility can also vary with pH levels, especially in biological systems where the protonation state of the carbamate group may impact overall solubility.

In summary, while [2-(2-chlorophenyl)-1-methyl-ethyl] carbamate may not be highly soluble in water, its polar nature allows for solubility in various organic solvents, making it a versatile compound in chemical applications. As is often quoted in the field of chemistry, “like dissolves like,” emphasizing the importance of understanding the solvent characteristics when working with such compounds.

Interesting facts

Interesting Facts about [2-(2-Chlorophenyl)-1-Methyl-Ethyl] Carbamate

[2-(2-Chlorophenyl)-1-Methyl-Ethyl] carbamate is a fascinating compound, notable for its biological and chemical significance. This compound is a member of the carbamate family, which are widely recognized for their applications in various fields, including agriculture and pharmaceuticals.

Key Highlights:

  • Applications in Agriculture: Compounds like this one are often utilized as pesticides. Their ability to control pest populations makes them invaluable in agricultural practices.
  • Enzyme Inhibition: [2-(2-Chlorophenyl)-1-Methyl-Ethyl] carbamate can act as a cholinesterase inhibitor, which means it interferes with the enzyme that breaks down acetylcholine, a critical neurotransmitter in the body.
  • Research Significance: This compound is of interest in biochemical research, particularly in studying mechanisms of action of neurotoxic compounds and understanding how certain chemicals affect neurological functions.
  • Synthetic Pathways: The synthetic routes to produce this compound can vary, often involving multi-step reactions that highlight the complexity and intricacies of organic synthesis.

As a student or scientist, studying compounds like [2-(2-Chlorophenyl)-1-Methyl-Ethyl] carbamate unveils a deeper understanding of chemical interactions and the nuances of organic chemistry. Furthermore, the impact of such compounds on environmental and human health emphasizes the importance of responsible chemical usage and regulation.

In the words of a prominent chemist, "Every compound is a story waiting to be uncovered," and compounds like this indeed offer intriguing tales regarding their structure, function, and impact.

Synonyms
712-91-4
MH 1666
BRN 1875134
CARBAMIC ACID, o-CHLORO-alpha-METHYLPHENETHYL ESTER
SCHEMBL23347648
DTXSID10991516
JHZISMYMEAAHJP-UHFFFAOYSA-N
1-(2-Chlorophenyl)propan-2-yl hydrogen carbonimidate