Skip to main content

Acetochlor

ADVERTISEMENT
Identification
Molecular formula
C14H20ClNO2
CAS number
34256-82-1
IUPAC name
N-(2-chlorophenyl)-3-oxo-butanamide
State
State

Acetochlor is a liquid at room temperature. It is slightly viscous and has a low volatility.

Melting point (Celsius)
1.00
Melting point (Kelvin)
274.15
Boiling point (Celsius)
202.00
Boiling point (Kelvin)
475.15
General information
Molecular weight
221.67g/mol
Molar mass
221.6720g/mol
Density
1.1000g/cm3
Appearence

Acetochlor is a colorless to amber liquid at room temperature. It is often available as a formulation for agricultural use, typically emulsified in water. In its pure form, it is oily and has a mild characteristic odor.

Comment on solubility

Solubility of N-(2-chlorophenyl)-3-oxo-butanamide

N-(2-chlorophenyl)-3-oxo-butanamide, with its unique structure, exhibits distinct solubility characteristics that are noteworthy in various contexts. Understanding its solubility is crucial for applications in drug formulation, environmental studies, and chemical reactions. Let's delve into the key aspects of its solubility:

  • Polar vs. Non-polar: The presence of the 2-chlorophenyl group may enhance the polarity of the compound, potentially leading to a higher solubility in polar solvents such as water or ethanol.
  • Solvent Compatibility: This compound might show better solubility in organic solvents due to non-polar interactions, making it compatible with various organic reactions.
  • Temperature Dependence: Like many organic compounds, the solubility of N-(2-chlorophenyl)-3-oxo-butanamide can be affected by temperature changes—typically increasing with higher temperatures.
  • pH Influence: The solubility may also vary with pH levels, especially if the functional groups can become ionized.

In conclusion, the solubility of N-(2-chlorophenyl)-3-oxo-butanamide is influenced by its chemical structure and the surrounding environment. It is essential to consider these factors when investigating its applications and behavior in different media. As the saying goes, "A compound's true potential often lies in its interactions."

Interesting facts

Interesting Facts about N-(2-chlorophenyl)-3-oxo-butanamide

N-(2-chlorophenyl)-3-oxo-butanamide is a fascinating compound that lies at the intersection of organic chemistry and pharmaceutical applications. Here are some intriguing insights into this compound:

  • Structure and Functionality: This compound features a unique amide bond, which is a key characteristic of many biologically active molecules. The presence of the 2-chlorophenyl group enhances its potential as a selective pharmacological agent.
  • Biological Relevance: The compound is explored for its possible therapeutic effects, which include anti-inflammatory and analgesic properties. The chlorinated phenyl ring often increases the lipophilicity of compounds, making them more effective in crossing cell membranes.
  • Synthesis Pathways: It can be synthesized through various organic reactions, including acylation and condensation processes, showcasing the versatility of synthetic methodologies in organic chemistry.
  • Research Significance: Given its structure, N-(2-chlorophenyl)-3-oxo-butanamide has gained attention in drug design, specifically as a precursor for more advanced compounds that may exhibit enhanced biological activity.
  • Real-World Applications: Compounds with similar structures have already found their way into medications used to treat chronic pain and other related conditions, marking their significance in medicinal chemistry.

As a chemistry student or scientist, understanding compounds like N-(2-chlorophenyl)-3-oxo-butanamide not only enhances your knowledge but also provides insight into the practical applications of organic chemistry in healthcare.

In the words of renowned chemist Linus Pauling, "The best way to have a good idea is to have a lot of ideas." This compound exemplifies how innovative thinking can lead to discoveries that benefit society.

Synonyms
2'-Chloroacetoacetanilide
93-70-9
N-(2-Chlorophenyl)-3-oxobutanamide
AAoC
o-Chloroacetoacetanilide
Butanamide, N-(2-chlorophenyl)-3-oxo-
Acetoacet-o-chloroanilide
N-Acetoacetyl-2-chloroaniline
Acetoacetyl-2-chloroanilide
Acetoacetyl-o-chloroanilide
Acetoacet-o-chloranilide
o-Acetoacetochloroanilide
N-(2-Chlorophenyl)acetoacetamide
o-Acetoacetochloranilide
Acetoacet-o-chloroacetanilide
Acetoacetanilide, o-chloro-
ACETOACETANILIDE, 2'-CHLORO-
NSC 3913
3-Oxo-N-(2-chlorophenylbutanamide)
Butaneamide, N-(2-chlorophenyl)-3-oxo-
EINECS 202-269-1
BRN 2212748
5KXO30B5F8
Acetoacetic acid 2-chloroanilide
AI3-01927
NSC-3913
acetoacetic acid o-chloroanilide
DTXSID9052630
BFVHBHKMLIBQNN-UHFFFAOYSA-
EC 202-269-1
4-12-00-01133 (Beilstein Handbook Reference)
N-(2-Chlorophenyl)-3-oxo-butyramide
Maybridge1_002473
UNII-5KXO30B5F8
DivK1c_001225
SCHEMBL300285
DTXCID6031203
HMS548I09
NSC3913
ALBB-013685
N-(2-Chlorophenyl)-3-oxobutyramide
BTB 13411
CCG-45974
MFCD00018224
STK397824
AKOS000313207
N-(2-Chlorophenyl)-3-oxobutanamide #
CDS1_000185
DB-057423
NS00005749
F79758
N~1~-(2-CHLOROPHENYL)-3-OXOBUTANAMIDE
12G-917
SR-01000635707-1
Q27895410
Z56771094
202-269-1