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Oxalyl chloride

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Identification
Molecular formula
C2Cl2O2
CAS number
79-37-8
IUPAC name
(2-chlorophenyl)methyl-[2-[[8-[2-[(2-chlorophenyl)methyl-diethyl-ammonio]ethylamino]-8-oxo-octanoyl]amino]ethyl]-diethyl-ammonium;dichloride
State
State

Oxalyl chloride is typically found as a liquid at room temperature. Due to its reactive nature, it is seldom encountered outside controlled environments.

Melting point (Celsius)
-10.00
Melting point (Kelvin)
263.15
Boiling point (Celsius)
63.00
Boiling point (Kelvin)
336.15
General information
Molecular weight
126.93g/mol
Molar mass
126.9270g/mol
Density
1.4320g/cm3
Appearence

Oxalyl chloride is a colorless to pale yellow liquid with a sharp, pungent odor. It is corrosive and reacts violently with water, producing hydrochloric acid and oxalic acid as decomposition products. It is often handled in a fume hood due to the release of hazardous gases.

Comment on solubility

Solubility of (2-chlorophenyl)methyl-[2-[[8-[2-[(2-chlorophenyl)methyl-diethyl-ammonio]ethylamino]-8-oxo-octanoyl]amino]ethyl]-diethyl-ammonium;dichloride

The solubility of the compound (2-chlorophenyl)methyl-[2-[[8-[2-[(2-chlorophenyl)methyl-diethyl-ammonio]ethylamino]-8-oxo-octanoyl]amino]ethyl]-diethyl-ammonium;dichloride can significantly vary depending on several factors. Typically, quaternary ammonium salts like this one are known for their high solubility in polar solvents. Here are some factors to consider regarding its solubility:

  • Nature of the solvent: This compound is likely soluble in water due to the presence of ammonium groups that can interact favorably with polar water molecules.
  • Temperature: As with many ionic compounds, an increase in temperature typically enhances solubility, allowing for a greater interaction between solute and solvent.
  • Concentration: Depending on the concentration of the compound in the solvent, solubility may reach saturation, leading to limited further dissolution.
  • pH of the solution: The solubility of this compound could also be pH-dependent, particularly if it can exist in different ionization states under varying conditions.

In summary, while (2-chlorophenyl)methyl-[2-[[8-[2-[(2-chlorophenyl)methyl-diethyl-ammonio]ethylamino]-8-oxo-octanoyl]amino]ethyl]-diethyl-ammonium;dichloride is expected to be soluble in aqueous environments, specific testing is essential to determine the precise solubility under various conditions.

Interesting facts

Interesting Facts About (2-chlorophenyl)methyl-[2-[[8-[2-[(2-chlorophenyl)methyl-diethyl-ammonio]ethylamino]-8-oxo-octanoyl]amino]ethyl]-diethyl-ammonium;dichloride

The compound known as (2-chlorophenyl)methyl-[2-[[8-[2-[(2-chlorophenyl)methyl-diethyl-ammonio]ethylamino]-8-oxo-octanoyl]amino]ethyl]-diethyl-ammonium;dichloride is a fascinating entity in the realm of medicinal chemistry and pharmacology. Here are some engaging facts about this complex molecule:

  • Quaternary Ammonium Compound: This compound features a quaternary ammonium structure, which often grants it interesting biological properties, particularly in its ability to penetrate biological membranes and interact with cellular targets.
  • Biological Applications: Due to its unique structure, compounds like this may serve as important targets for drug design, especially in areas such as cancer therapy or antimicrobial development.
  • Chlorophenyl Groups: The presence of chlorophenyl substituents suggests potential activity in modulating biological pathways, as halogenated phenyl groups often show enhanced binding affinity to biomolecular targets.
  • Amphiphilic Nature: The combination of hydrophilic and hydrophobic components within its structure may allow this compound to act as a surfactant, thereby affecting its behavior in biological systems.
  • Structural Complexity: The intricate arrangement of moieties highlights the significance of structural modifications in tuning the pharmacological profiles of similar compounds, making it an excellent study subject for synthetic chemists.

In summary, this compound exemplifies how intricate chemical structures can lead to significant biomedical applications. Its ability to influence biological systems opens up many avenues for research and development.

Synonyms
(Suberoylbis(iminoethylene))bis((o-chlorobenzyl)diethylammonium chloride)
AMMONIUM, (SUBEROYLBIS(IMINOETHYLENE))BIS((o-CHLOROBENZYL)DIETHYL-, DICHLORIDE
15947-92-9