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Chlorpyrifos

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Identification
Molecular formula
C8H6Cl4NO
CAS number
5598-13-0
IUPAC name
2-chloro-N-(2,4,6-trichlorophenyl)acetamide
State
State

At room temperature, this compound maintains a solid state. It remains stable under standard conditions and does not easily transition to other states without the application of heat or dissolution in solvents.

Melting point (Celsius)
104.50
Melting point (Kelvin)
377.65
Boiling point (Celsius)
360.00
Boiling point (Kelvin)
633.15
General information
Molecular weight
296.46g/mol
Molar mass
296.4580g/mol
Density
1.5900g/cm3
Appearence

The compound is a white to off-white crystalline solid. It appears as a crystalline powder and can have a faint chemical odor. The crystals might vary in size but remain consistent in their solid-state format.

Comment on solubility

Solubility of 2-chloro-N-(2,4,6-trichlorophenyl)acetamide

The solubility of 2-chloro-N-(2,4,6-trichlorophenyl)acetamide can be quite intriguing due to its chemical structure and the presence of multiple chlorinated aromatic groups. Understanding its solubility characteristics is essential for applications in various chemical processes.

Key Points on Solubility:

  • Polarity: This compound is likely to have low polarity due to the presence of chlorine substituents, which generally do not enhance solubility in polar solvents.
  • Solvent Compatibility: It is expected to be more soluble in organic solvents, such as acetone or chloroform, rather than in water.
  • Temperature Effects: Solubility may increase with an increase in temperature, which is common for many organic compounds.
  • Structural Influence: The bulky trichlorophenyl group may hinder solvation, thus affecting overall solubility in various solvents.

In summary, while the specific solubility of 2-chloro-N-(2,4,6-trichlorophenyl)acetamide may not be readily available in standard references, its structural characteristics suggest a preference for organic solvents. As with many chlorinated compounds, its solubility behavior can play a significant role in its reactivity and applications in synthesis or biochemistry.

Interesting facts

Interesting Facts about 2-chloro-N-(2,4,6-trichlorophenyl)acetamide

2-chloro-N-(2,4,6-trichlorophenyl)acetamide is a notable example of a compound that finds its significance in various fields, particularly in the agricultural and pharmaceutical industries. This compound is part of the larger family of chloroacetamides, which are recognized for their herbicidal properties.

Key Features

  • Herbicide Properties: This compound has been utilized as a selective herbicide, effectively controlling a range of weed species while leaving crops unharmed.
  • Mode of Action: It acts by inhibiting specific enzymatic pathways in plants, leading to the disruption of growth and ultimately causing weed death.
  • Environmental Impact: Understanding the environmental effects of chloroacetamide compounds is crucial, as their persistence in soil and potential runoff into water systems can affect ecosystems.
  • Pharmaceutical Potential: Beyond agriculture, researchers have investigated similar compounds for their biological activity, exploring their potential in medicinal chemistry.

Historical Context

This compound is part of a class of chemicals that emerged in the mid-20th century, coinciding with advancements in synthetic organic chemistry. As farmers sought more effective methods for crop management, compounds like 2-chloro-N-(2,4,6-trichlorophenyl)acetamide became pivotal.

Safety and Regulation

With its applications in agriculture, regulatory bodies closely monitor this compound to ensure that its use does not pose a risk to human health or the environment. Compliance with guidelines and studying its long-term effects are essential considerations for scientists working in this domain.

In summary, 2-chloro-N-(2,4,6-trichlorophenyl)acetamide exemplifies the complex interplay between chemical innovation, agricultural practice, and environmental stewardship. As research continues, its role and applications may evolve, underscoring the importance of ongoing scientific inquiry in understanding chemical compounds.

Synonyms
2-chloro-N-(2,4,6-trichlorophenyl)acetamide
22303-34-0
ACETANILIDE, 2,2',4',6'-TETRACHLORO-
7VUY278PXX
2',4',6'-Trichloro-2-chloroacetanilide
NSC-159614
DTXSID10176846
4-12-00-01282 (Beilstein Handbook Reference)
RefChem:86390
DTXCID3099337
PXPBIOJVDMLMKK-UHFFFAOYSA-N
2,2',4',6'-Tetrachloroacetanilide
2-Chloro-N-(2,4,6-trichloro-phenyl)-acetamide
Acetamide, 2-chloro-N-(2,4,6-trichlorophenyl)-
Acetamide,2-chloro-N-(2,4,6-trichlorophenyl)-
NSC 159614
BRN 1247904
NSC159614
UNII-7VUY278PXX
WLN: G1VMR BG DG FG
SCHEMBL7810747
2,4',6'-Tetrachloroacetanilide
Acetamide,4,6-trichlorophenyl)-
alpha,2,4,6-Tetrachloroacetanilide
XAA30334
MFCD00018890
STK118522
Acetanilide,2',4',6'-tetrachloro-
AKOS000283719
NCGC00661079-01
CS-0218655
ST50214163
EN300-01625
G45945
Z56867324