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Iodophenyl Acetate (example compound name)

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Identification
Molecular formula
C15H10ClI2NO3
CAS number
25684-01-3
IUPAC name
[2-[(4-chlorophenyl)carbamoyl]-4,6-diiodo-phenyl] acetate
State
State

At room temperature, the compound is a solid, typically found in a crystalline powder form. It is known for its stability under normal conditions.

Melting point (Celsius)
108.00
Melting point (Kelvin)
381.15
Boiling point (Celsius)
342.00
Boiling point (Kelvin)
615.15
General information
Molecular weight
515.52g/mol
Molar mass
515.5230g/mol
Density
3.1678g/cm3
Appearence

The compound typically appears as a white to off-white crystalline powder.

Comment on solubility

Solubility of [2-[(4-chlorophenyl)carbamoyl]-4,6-diiodo-phenyl] acetate

The solubility of [2-[(4-chlorophenyl)carbamoyl]-4,6-diiodo-phenyl] acetate in various solvents can provide insights into its chemical behavior and potential applications. Here are some key considerations:

  • Polar Solvents: Generally, compounds with polar functional groups tend to have higher solubility in polar solvents like water and alcohols. In this case, the presence of the carbamoyl group may enhance solubility in polar environments.
  • Non-polar Solvents: Conversely, due to its significant aromatic character and halogenation (iodine and chlorine atoms), the compound might display enhanced solubility in non-polar solvents such as hexane or toluene.
  • Hydrogen Bonding: The potential for hydrogen bonding (stemming from the carbamoyl group) may lead to increased solubility in solvents capable of such interactions, providing an additional layer of complexity.
  • Effect of Iodine: The presence of multiple iodine atoms might affect the overall solubility profile, as iodine atoms can introduce steric hindrances and alter intermolecular interactions.

In conclusion, understanding the solubility of [2-[(4-chlorophenyl)carbamoyl]-4,6-diiodo-phenyl] acetate is essential for its practical applications, influencing aspects such as formulation in drug development and material science. Experimentation in different solvents will provide the most accurate insight into its behavior.

Interesting facts

Interesting Facts about 2-[(4-chlorophenyl)carbamoyl]-4,6-diiodo-phenyl Acetate

This intriguing compound, known as 2-[(4-chlorophenyl)carbamoyl]-4,6-diiodo-phenyl acetate, showcases a unique combination of functional groups and halogen substitutions that play essential roles in its chemical behavior and potential applications. Here are some engaging insights:

  • Versatile Uses: Due to its structural properties, this compound may exhibit significant biological activity and could be investigated for its potential pharmaceutical applications.
  • Structural Complexity: The presence of both chloro and iodo substituents in the aromatic rings can lead to interesting electronic effects, making this compound an excellent subject for studying substituent effects on reactivity and stability.
  • Synthetic Routes: The synthesis of compounds with such halogenated phenyl groups often involves intricate multi-step reactions, showcasing the creativity and skill required in organic synthesis.
  • Research Potential: The study of halogenated compounds like this one is critical in materials science and medicinal chemistry, as halogen atoms can influence lipophilicity and biological interactions.
  • Environmental Considerations: Given the presence of halogens, it is essential to study the environmental impact and degradation pathways of such compounds, particularly in the context of sustainability and toxicology.

The exploration of 2-[(4-chlorophenyl)carbamoyl]-4,6-diiodo-phenyl acetate not only enriches our understanding of chemical compounds but also highlights the ongoing need to evaluate the implications of their use in various fields. The exciting interplay between chemistry and potential applications continues to propel research forward, making compounds like this profound subjects of inquiry for scientists and students alike.

Synonyms
CLIOXANIDE
14437-41-3
Clioxanida
Clioxanidum
CN 59,567
Benzamide, 2-(acetyloxy)-N-(4-chlorophenyl)-3,5-diiodo-
SYD-230
4'-Chloro-3,5-diiodosalicylanilide acetate
CI-633
CN 59567
NSC-233846
2-(Acetyloxy)-N-(4-chlorophenyl)-3,5-diiodobenzamide
2Q9A409N0B
CN-59567
DTXSID1065766
DTXCID0034695
238-414-0
Tremerad
SYD 230
2-Acetoxy-3,5-diiodo-4'-chlorobenzanilide
2-Acetoxy-4'-chloro-3,5-di-iodobenzanilide
2-(4-Chlorphenylcarbamoyl)-4,6-diodphenyl acetat
MLS001249435
[2-[(4-chlorophenyl)carbamoyl]-4,6-diiodophenyl] acetate
NSC 233846;SYD 230;Tremerad
SMR000718656
2-[(4-CHLOROANILINO)CARBONYL]-4,6-DIIODOPHENYL ACETATE
Clioxanidum [INN-Latin]
Clioxanida [INN-Spanish]
EINECS 238-414-0
NSC 233846
BRN 2950514
Acetoxy-4'-chloro-3,5-diiodobenzanilide
C.I. 633
Clioxanide [USAN:INN:BAN]
UNII-2Q9A409N0B
CL 633
Salicylanilide, 4'-chloro-3,5-diiodo-, acetate ester
Benzanilide, 4'-chloro-3,5-diiodo-2-hydroxy-, acetate
CLIOXANIDE [MI]
CLIOXANIDE [INN]
Clioxanide (USAN/INN)
CLIOXANIDE [USAN]
CBDivE_009451
cid_26695
MLS001249506
SCHEMBL636665
CHEMBL236150
orb1697761
SCHEMBL29358452
BDBM76289
ICKMASVVMCGZLR-UHFFFAOYSA-N
MFCD00552914
NSC233846
AKOS001584706
Salicylanilide,5-diiodo-, acetate ester
NCGC00245804-01
Benzanilide,5-diiodo-2-hydroxy-, acetate
C.I.-633
Salicylanilide,5-diiodo-, acetate (ester)
HY-114969
CS-0064710
NS00021012
D03539
Q27255474
[2-[(4-chlorophenyl)carbamoyl]-4,6-bis(iodanyl)phenyl] ethanoate
acetic acid [2-[(4-chloroanilino)-oxomethyl]-4,6-diiodophenyl] ester
acetic acid [2-[(4-chlorophenyl)carbamoyl]-4,6-diiodo-phenyl] ester