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Bamisant

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Identification
Molecular formula
C10H11Cl3NO3
CAS number
51035-46-8
IUPAC name
[2,2-dichloro-3-(4-chlorophenyl)-3-hydroxy-propyl] carbamate
State
State

At room temperature, this compound is typically a crystalline solid.

Melting point (Celsius)
117.00
Melting point (Kelvin)
390.15
Boiling point (Celsius)
350.00
Boiling point (Kelvin)
623.15
General information
Molecular weight
274.56g/mol
Molar mass
274.6150g/mol
Density
1.4200g/cm3
Appearence

This compound appears as a white crystalline solid.

Comment on solubility

Solubility of [2,2-dichloro-3-(4-chlorophenyl)-3-hydroxy-propyl] carbamate

The solubility of [2,2-dichloro-3-(4-chlorophenyl)-3-hydroxy-propyl] carbamate is a significant aspect to consider for its application and functionality. This compound is typically characterized by its structural complexity and the presence of various functional groups.

Key Aspects of Solubility:

  • Polarity: The presence of hydroxyl (–OH) groups often enhances solubility in polar solvents, predominantly water. However, the chlorinated phenyl groups can introduce hydrophobic characteristics, possibly leading to lower overall solubility.
  • pH Dependence: The solubility may vary with pH changes. At different pH levels, the ionization state of the hydroxyl or carbamate groups could influence solubility, making it more soluble in certain conditions.
  • Solvent Compatibility: This compound may exhibit varying solubility in organic solvents such as ethanol or acetone, enhancing its versatility for different applications.

In summary, while [2,2-dichloro-3-(4-chlorophenyl)-3-hydroxy-propyl] carbamate demonstrates potential solubility in polar environments due to hydroxyl functionality, the overall solubility profile must be carefully evaluated based on solvent choice and environmental conditions. This evaluation is crucial for understanding its behavior in various chemical applications.

Interesting facts

Interesting Facts about [2,2-dichloro-3-(4-chlorophenyl)-3-hydroxy-propyl] carbamate

[2,2-dichloro-3-(4-chlorophenyl)-3-hydroxy-propyl] carbamate is a fascinating compound that has garnered attention in the field of agricultural chemistry, particularly in the development of pesticides and herbicides. This compound features a unique structure that includes both chlorine and hydroxyl functional groups, which contribute to its biological activity. Below are some remarkable insights into this chemical:

  • Mechanism of Action: This compound operates by interfering with key biological pathways in pests, making it effective in controlling unwanted plant and animal species.
  • Environmental Impact: Understanding the environmental fate of such compounds is crucial as they can have varying levels of persistence in ecosystems, influencing both non-target species and soil health.
  • Applications in Research: Scientists often utilize compounds like this one to study the effects of chlorinated substances on various metabolic pathways, providing valuable insights into toxicology and biochemistry.
  • Regulatory Scrutiny: Given its chlorinated nature, this compound may be subject to regulatory review due to potential health and ecological risks associated with chlorinated organic compounds.

As a candidate in the ongoing research for safer and more efficient agricultural practices, [2,2-dichloro-3-(4-chlorophenyl)-3-hydroxy-propyl] carbamate stands as a testament to the interplay between chemistry and the environment. Its multifaceted role highlights the need for responsible usage and development of chemical solutions that prioritize environmental sustainability.

In summary, as we further explore compounds like [2,2-dichloro-3-(4-chlorophenyl)-3-hydroxy-propyl] carbamate, it is essential to balance productivity with ecological responsibility.

Synonyms
1477-41-4
[2,2-dichloro-3-(4-chlorophenyl)-3-hydroxypropyl] carbamate
SQ-10220
SQ 10,220
G1T3F37VUR
Carbamic acid 2,2-dichloro-3-(p-chlorophenyl)-3-hydroxypropyl ester
UNII-G1T3F37VUR
CARBAMIC ACID, 3-p-CHLOROPHENYL-2,2-DICHLORO-3-HYDROXYPROPYL ESTER
SQ 10220
1,3-Propanediol, 2,2-dichloro-1-(4-chlorophenyl)-, 3-carbamate
2,2-Dichloro-1-(p-chlorophenyl)-1,3-propanediol-O(sup 3)-carbamate
3-p-Chlorophenyl-2,2-dichloro-3-hydroxypropyl ester of carbamic acid
DTXSID30933190
Carbamic acid, 2,2-dichloro-3-(p-chlorophenyl)-3-hydroxypropyl ester
Q27278614
[2,2-Dichloro-3-(4-chlorophenyl)-3-hydroxypropyl]carbamate
2,2-Dichloro-3-(4-chlorophenyl)-3-hydroxypropyl hydrogen carbonimidate