Skip to main content

4,4′-Dichlorodiphenyl trichloroethane

ADVERTISEMENT
Identification
Molecular formula
C14H9Cl5
CAS number
50-29-3
IUPAC name
(4-chlorophenyl)-(4-chlorophenyl)imino-oxido-ammonium
State
State

At room temperature, the compound is in a solid state, appearing as a crystalline powder.

Melting point (Celsius)
109.00
Melting point (Kelvin)
382.15
Boiling point (Celsius)
260.00
Boiling point (Kelvin)
533.15
General information
Molecular weight
354.49g/mol
Molar mass
354.4900g/mol
Density
1.5000g/cm3
Appearence

The compound typically appears as a white crystalline solid. It is colorless and does not have a pronounced odor.

Comment on solubility

Solubility of (4-chlorophenyl)-(4-chlorophenyl)imino-oxido-ammonium

The solubility of the compound (4-chlorophenyl)-(4-chlorophenyl)imino-oxido-ammonium can be quite specific due to its unique structure. Here are some key points regarding its solubility:

  • Polar Nature: This compound contains polar functional groups, which can lead to increased solubility in polar solvents like water.
  • Solubility in Organic Solvents: Conversely, its chlorinated phenyl groups may enhance solubility in non-polar organic solvents such as benzene and toluene.
  • Intramolecular Interactions: The presence of nitrile and amine interactions can potentially affect solubility, possibly making it less soluble in extreme pH environments.
  • Temperature Dependency: As with many chemicals, solubility may improve with an increase in temperature, allowing more effective dissolution.

Overall, the solubility of (4-chlorophenyl)-(4-chlorophenyl)imino-oxido-ammonium will depend on the solvent environment, temperature, and the specific interactions between the compound and solvent molecules. As stated, "Like dissolves like," hence understanding the nature of both the compound and solvent is crucial for predicting solubility behavior.

Interesting facts

Interesting Facts about (4-Chlorophenyl)-(4-chlorophenyl)imino-oxido-ammonium

(4-Chlorophenyl)-(4-chlorophenyl)imino-oxido-ammonium is a fascinating chemical compound that showcases the intricacies of nitrogen-oxygen bonding in organic compounds. Here are some notable points about this compound:

  • Innovative Applications: This compound is often explored for its potential use in various industrial applications, particularly in the field of agrochemicals and pharmaceuticals.
  • Unique Structure: The presence of both 4-chlorophenyl groups contributes to its stability and reactivity, making it an interesting subject of study for chemists looking to understand substituent effects on chemical properties.
  • Research Potential: The nitrogen-oxygen interaction in its structure positions it as a candidate for studies on nitrogen oxides and their role in environmental chemistry, as well as their behavior in biological systems.
  • Chirality Considerations: The specific arrangement of substituents in this compound could lead to chiral forms, which are significant in the synthesis of chirally pure drugs that have better efficacy and reduced side effects.
  • Synthetic Pathways: The synthesis of this compound typically involves intricate multi-step reactions, a process that allows students and researchers to engage in deeper discussions about reaction mechanisms and organic synthesis techniques.

In essence, (4-chlorophenyl)-(4-chlorophenyl)imino-oxido-ammonium provides a rich ground for exploration in both theoretical and applied chemistry. Its fascinating structure and potential applications make it a compound that beckons further study and discussion within the scientific community.

Synonyms
4,4'-DICHLOROAZOXYBENZENE
614-26-6
Dcaob
Azoxybenzene, 4,4'-dichloro-
p,p'-Dichloroazoxybenzene
HSDB 2721
Diazene, bis(4-chlorophenyl)-, 1-oxide
Bis(4-chlorphenyl)diazene 1-oxide
Bis(4-chlorophenyl)diazene 1-oxide
NSC 166795
BRN 0656043
AI3-03276
Diazene, bis(4-chlorphenyl)-, 1-oxide
DTXSID3073210
4-16-00-00035 (Beilstein Handbook Reference)
8X82KV0420
NSC-166795
p,p'Dichloroazoxybenzene
Azoxybenzene, 4,4'dichloro
Bis(4chlorphenyl)diazene 1oxide
DTXCID3043021
Bis(4chlorophenyl)diazene 1oxide
Diazene, bis(4chlorophenyl), 1oxide
Diazene, bis(4-chlorphenyl)-, 1-oxide (9CI)
BIS(4-CHLOROPHENYL)DIAZENE 1-OXIDE [HSDB]
DIAZENE, 1,2-BIS(4-CHLOROPHENYL)-, 1-OXIDE
636-408-6
(4-chlorophenyl)-(4-chlorophenyl)imino-oxidoazanium
trans-4,4'-Dichloroazoxybenzene
4,4'-Dichloroazoxybenzene, (E)-
4,4'-Dichloroazoxybenzene, (Z)-
21650-66-8
CAV0B510XV
WH8662LY1J
Diazene, bis(4-chlorophenyl)-, 1-oxide, (Z)-
Diazene, bis(4-chlorophenyl)-, 1-oxide, (1Z)-
Diazene, 1,2-bis(4-chlorophenyl)-, 1-oxide, (1Z)-
(Z)-1,2-Bis(4-chlorophenyl)diazene 1-oxide
71297-93-3
UNII-CAV0B510XV
UNII-8X82KV0420
Azoxybenzene,4'-dichloro-
UNII-WH8662LY1J
44DICHLOROAZOXYBENZENE
YSZC3202
(E)-4,4'-dichloroazoxybenzene
(Z)-4,4'-dichloroazoxybenzene
amino(4-chlorophenyl)[(4-chlorophenyl)azamethylene]-1-ol
NMAZIJPSESMWSA-UHFFFAOYSA-N
MFCD00018597
NSC166795
AKOS003368406
CIS-4,4'-DICHLOROAZOXYBENZENE
FD66253
Azoxybenzene, 4,4'-dichloro-, trans-
Azoxybenzene, 4,4'-dichloro-, trans-,
1,2-Bis(4-chlorophenyl)diazene 1-oxide
AZOXYBENZENE, 4,4'-DICHLORO-, (E)-
1,2-di(4-chlorophenyl)diaz-1-en-1-ium-1-olate
Q27275381
Q27292633
DIAZENE, BIS(4-CHLOROPHENYL)-, 1-OXIDE, (E)-