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Propanil

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Identification
Molecular formula
C10H9ClNO2
CAS number
709-98-8
IUPAC name
2-(4-chlorophenoxy)-N'-isopropyl-acetohydrazide
State
State

At room temperature, propanil is found in a solid state. The state may vary slightly depending on ambient conditions and pressure, but it generally remains solid under standard conditions. It is mainly used in agricultural settings where it is applied in the form of a wettable powder or emulsifiable concentrate.

Melting point (Celsius)
93.50
Melting point (Kelvin)
366.65
Boiling point (Celsius)
315.80
Boiling point (Kelvin)
588.95
General information
Molecular weight
218.66g/mol
Molar mass
218.6560g/mol
Density
1.3150g/cm3
Appearence

Propanil is typically a colorless to white solid in its pure form. It may appear as a crystalline powder which is often odorless. Impurities or formulations can impart different colors, but these are not characteristic of its pure state.

Comment on solubility

Solubility Overview of 2-(4-chlorophenoxy)-N'-isopropyl-acetohydrazide

The solubility of 2-(4-chlorophenoxy)-N'-isopropyl-acetohydrazide can be a complex topic due to its varied interactions with solvents. Generally, the solubility characteristics of this compound can be influenced by several key factors:

  • Polarity: The presence of the 4-chlorophenoxy group may impart some degree of polarity, affecting how the compound interacts with polar solvents like water.
  • Hydrophobic Character: The isopropyl group contributes a hydrophobic character, which can limit solubility in highly polar environments.
  • Temperature: As with many organic compounds, solubility can improve with increased temperature, promoting better interaction with solvents.
  • pH: Changes in pH can also affect solubility by influencing ionization states of functional groups.

Furthermore, it is essential to consider common solvents for this type of compound:

  • Organic Solvents: Compounds like ethanol, methanol, or dimethyl sulfoxide (DMSO) may enhance solubility.
  • Aqueous Solutions: Water solubility is generally limited, potentially making this compound less soluble in aqueous environments.

In conclusion, understanding the solubility of 2-(4-chlorophenoxy)-N'-isopropyl-acetohydrazide requires a careful assessment of its chemical structure and the environment in which it is placed. As the famous saying goes, "Like dissolves like," illustrating the importance of molecular compatibility in solubility.

Interesting facts

Interesting Facts about 2-(4-chlorophenoxy)-N'-isopropyl-acetohydrazide

2-(4-chlorophenoxy)-N'-isopropyl-acetohydrazide is a fascinating chemical compound that showcases the versatility of hydrazide structures in organic chemistry. Here are some intriguing aspects of this compound:

  • Biological Significance: Compounds like 2-(4-chlorophenoxy)-N'-isopropyl-acetohydrazide are often studied for their potential biological activities. Hydrazide derivatives can exhibit properties such as antibacterial, antifungal, and anti-inflammatory effects, making them valuable in pharmaceutical research.
  • Functional Groups: The presence of both the chlorophenoxy and hydrazide functionalities contributes to the compound's reactivity and interaction with various biological targets, allowing for diverse applications in medicinal chemistry.
  • Synthesis Techniques: The synthesis of this compound involves skilled techniques such as nucleophilic substitution reactions. Understanding the mechanism behind these reactions can enhance the efficacy of creating similar compounds.
  • Structure-Activity Relationship (SAR): The design of hydrazide compounds allows chemists to explore SAR, which is crucial for optimizing the properties of potential drug candidates. Small modifications to the structure can lead to significant changes in biological activity.
  • Environmental Role: Chlorinated compounds often have important roles in environmental chemistry, where they can be used to study their impact on ecosystems and bioremediation efforts.

In summary, 2-(4-chlorophenoxy)-N'-isopropyl-acetohydrazide is not only a compound of interest in the lab but also a potential key player in the development of new therapeutic agents. Its unique structure and properties make it an exemplary subject for both academic and applied research in the realm of chemistry.

Synonyms
Iproclozide
Iproclozid
3544-35-2
Iproclozida
Sinderesin
Sursum
Iproclozidum
SOG-4
Iproclozide [INN:BAN:DCF]
Iproclozidum [INN-Latin]
Iproclozida [INN-Spanish]
UNII-1II9D6CB3J
EINECS 222-589-5
1II9D6CB3J
Iproclozide (TN)
PC-603
Iproclozide (INN)
BRN 2119215
IPROCLOZIDE [MI]
p-Chlorophenoxyacetic acid 2-isopropylhydrazide
IPROCLOZIDE [INN]
1-(p-Chlorophenoxyacetyl)-2-isopropyl hydrazine
(p-Chlorophenoxy)acetic acid 2-isopropylhydrazide
IPROCLOZIDE [MART.]
IPROCLOZIDE [WHO-DD]
Isopropilidrazide dell'ac. p-cloro-fenossiacetico [Italian]
Acetic acid, (4-chlorophenoxy)-, 2-(1-methylethyl)hydrazide
ACETIC ACID, (p-CHLOROPHENOXY)-, 2-ISOPROPYLHYDRAZIDE
Isopropyl hydrazide de l'acide p-chlorophenoxyacetique [French]
DTXSID70188925
Isopropilidrazide dell'ac. p-cloro-fenossiacetico
Isopropyl hydrazide de l'acide p-chlorophenoxyacetique
(4-Chlorophenoxy)acetic acid 2-(1-methylethyl)hydrazide
Iproclozidum (INN-Latin)
Iproclozida (INN-Spanish)
IPROCLOZIDE (MART.)
2-(4-chlorophenoxy)-N'-(propan-2-yl)acetohydrazide
DTXCID30111416
N06AF06
p-(chlorophenoxy)acetic acid 2-isopropylhydrazide
Acetic acid, (4-chlorophenoxy)-, 2-(1-methylethyl)hydrazide (9CI)
222-589-5
pc 603
Iproclozid; PC 603; PU 603; Sursum
2-(4-chlorophenoxy)-N/'-propan-2-ylacetohydrazide
2-(4-chlorophenoxy)-N'-propan-2-ylacetohydrazide
2-(4-chlorophenoxy)-n'-isopropylacetohydrazide
SCHEMBL49744
CHEMBL91238
CHEBI:134988
GGECDTUJZOXAAR-UHFFFAOYSA-N
GLXC-02863
AKOS001592893
DB09247
NS00029857
D07338
2-(4-Chlorophenoxy)-N'-isopropyl-acetohydrazide
SR-01000078303
Q6065438
SR-01000078303-1