Skip to main content

Dichlofluanid

ADVERTISEMENT
Identification
Molecular formula
C13H12Cl2N4O2S
CAS number
1085-98-9
IUPAC name
[5-(3,5-dichlorophenyl)sulfanyl-4-isopropyl-1-(4-pyridylmethyl)imidazol-2-yl]methyl carbamate
State
State

At room temperature, dichlofluanid is typically found in a solid state. It is a stable compound under normal conditions, and its solid form makes it suitable for use as a fungicide in various agriculture and horticulture applications.

Melting point (Celsius)
75.00
Melting point (Kelvin)
348.15
Boiling point (Celsius)
451.00
Boiling point (Kelvin)
724.15
General information
Molecular weight
436.23g/mol
Molar mass
436.3000g/mol
Density
1.5400g/cm3
Appearence

Dichlofluanid is a solid powder that is white or slightly beige in color. It has a characteristic chemical odor, which is not particularly strong but is distinct enough to be noticeable.

Comment on solubility

Solubility of [5-(3,5-dichlorophenyl)sulfanyl-4-isopropyl-1-(4-pyridylmethyl)imidazol-2-yl]methyl carbamate

The solubility of the compound [5-(3,5-dichlorophenyl)sulfanyl-4-isopropyl-1-(4-pyridylmethyl)imidazol-2-yl]methyl carbamate, with the chemical formula C13H12Cl2N4O2S, presents notable aspects that are influenced by its structural features.

Here are some key points regarding its solubility:

  • Polarity: Due to the presence of multiple functional groups (such as carbamate and imidazole), this compound likely exhibits polar characteristics.
  • Hydrophobic and Hydrophilic Interactions: The dichlorophenyl and isopropyl groups contribute to hydrophobicity, while the pyridine ring introduces hydrophilicity, potentially resulting in a balanced solubility profile in various solvents.
  • Solvent Dependence: It may show varied solubility levels in organic solvents (e.g., dichloromethane, ethanol) compared to aqueous solutions, often preferring organic media.

As a result, when considering the application or use of this compound, it is crucial to analyze solubility under various conditions:

  1. Determine the solvent system that best dissolves the compound for desired experiments.
  2. Assess the impact of temperature on solubility, as it can significantly influence the dissolution process.
  3. Take into account the pH of the solution, which can affect the ionization of functional groups leading to changes in solubility.

To summarize, the solubility of [5-(3,5-dichlorophenyl)sulfanyl-4-isopropyl-1-(4-pyridylmethyl)imidazol-2-yl]methyl carbamate is intricate, reflecting a balance of polar and non-polar interactions that warrant careful consideration in both laboratory and practical applications.

Interesting facts

Interesting Facts about [5-(3,5-dichlorophenyl)sulfanyl-4-isopropyl-1-(4-pyridylmethyl)imidazol-2-yl]methyl carbamate

This compound is a fascinating example of combinatorial chemistry and medicinal applications. Its intricate structure showcases a unique combination of various functional groups, making it a subject of interest in pharmaceutical research. Here are a few captivating points:

  • Multi-faceted Structure: The presence of both imidazole and pyridine rings in the molecule enhances its potential for complex biochemical interactions, making it more versatile in targeting different biological pathways.
  • Biological Relevance: Compounds like this one are often synthesized for their biological activity, particularly in the fields of anticancer and antimicrobial research. Such derivatives may exhibit significant inhibitory effects against specific enzymes or receptors.
  • Dichlorophenyl Group: The incorporation of the 3,5-dichlorophenyl moiety is particularly notable for its role in modulating biological activity, often improving the compound's affinity towards target biomolecules.
  • Sulfanyl Group: The sulfanyl group is known for its ability to enhance solubility and stability, crucial factors when developing therapeutics. This group can also function as a leaving group in various chemical reactions.

In the words of a chemist, "The beauty of synthetic compounds lies not only in their structure but in the potential they hold for revolutionizing medicine." This compound exemplifies that concept, representing the intersection of chemistry, biology, and medicine. Its exploration could lead to breakthroughs in treating diseases that currently have limited therapeutic options.

Overall, [5-(3,5-dichlorophenyl)sulfanyl-4-isopropyl-1-(4-pyridylmethyl)imidazol-2-yl]methyl carbamate stands as a testament to the innovative possibilities present in modern chemical synthesis and drug development.

Synonyms
Capravirine
178979-85-6
AG 1549
AG-1549
S-1153
Capravirina
VHC779598X
CAPRAVIRINE [MI]
AG 549
AG1549
CAPRAVIRINE [INN]
S 1153
CAPRAVIRINE [USAN]
CAPRAVIRINE [WHO-DD]
DTXSID30170689
AGI 549; Capravirine; S 1153
2-Carbamoyloxymethyl-5-(3,5-dichlorophenylthio)-4-isopropyl-1-(pyridin-4-yl)methyl-1H-imidazole
1H-Imidazole-2-methanol, 5-((3,5-dichlorophenyl)thio)-4-(1-methylethyl)-1-(4-pyridinylmethyl)-, carbamate (ester)
(5-((3,5-dichlorophenyl)thio)-4-isopropyl-1-(pyridin-4-ylmethyl)-1H-imidazol-2-yl)methyl carbamate
[5-(3,5-dichlorophenyl)sulfanyl-4-propan-2-yl-1-(pyridin-4-ylmethyl)imidazol-2-yl]methyl carbamate
5-((3,5-Dichlorophenyl)thio)-4-isopropyl-1-(4-pyridylmethyl)imidazole-2-methanol carbamate (ester)
5-(3,5-dichlorophenyl)thio-4-isopropyl-1-(pyridin-4-yl-methyl)-1h-imidazol-2-yl-methyl carbamate
5-(3,5-Dichlorophenyl)thio-4-isopropyl-1-(4-pyridyl)methyl-1H-imidazol-2-ylmethyl carbamate
{5-[(3,5-dichlorophenyl)sulfanyl]-4-(propan-2-yl)-1-(pyridin-4-ylmethyl)-1H-imidazol-2-yl}methyl carbamate
capravirinum
UNII-VHC779598X
(5-((3,5-dichlorophenyl)sulfanyl)-4-(propan-2-yl)-1-(pyridin-4-ylmethyl)-1H-imidazol-2-yl)methyl carbamate
5-[(3,5-Dichlorophenyl)thio]-4-isopropyl-1-(4-pyridylmethyl)imidazole-2-methanol carbamate (ester)
CDIMI
Capravirine (USAN/INN)
Capravirine [USAN:INN]
SCHEMBL40347
S11
CHEMBL435128
DTXCID0093180
BDBM27579
YQXCVAGCMNFUMQ-UHFFFAOYSA-N
GLXC-02806
EX-A6254
AKOS040748084
DB08502
5-(3,5-dichlorophenyl)thio-4-isopropyl-1-(pyridin-4-yl)methyl-1H-imidazol-2-ylmethyl carbamate
HY-14294
DB-313861
NS00068309
D03371
Q5036216
Z2574923381
(5-(3,5-dichlorophenyl)sulfanyl-4-propan-2-yl-1-(pyridin-4-ylmethyl)imidazol-2-yl)methyl aminoformate
[5-(3,5-dichlorophenyl)sulfanyl-4-isopropyl-1-(4-pyridylmethyl)imidazol-2-yl]methyl carbamate
{5-[(3,5-dichlorophenyl)sulfanyl]-4-(1-methylethyl)-1-(pyridin-4-ylmethyl)-1H-imidazol-2-yl}methyl carbamate
5-(3,5-dichlorophenylthio)-4-isopropyl-1-(4-pyridylmethyl)-1H-imidazol-2-ylmethyl carbamate