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4-(4-chlorosulfonylphenoxy)benzenesulfonyl chloride

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Identification
Molecular formula
C12H8Cl2O4S2
CAS number
.Not Available
IUPAC name
4-(4-chlorosulfonylphenoxy)benzenesulfonyl chloride
State
State

At room temperature, the compound is in a solid state, appearing as crystalline powder. It is relatively stable under normal conditions but may react with bases, amines, and other nucleophiles.

Melting point (Celsius)
110.00
Melting point (Kelvin)
383.15
Boiling point (Celsius)
377.00
Boiling point (Kelvin)
650.15
General information
Molecular weight
357.22g/mol
Molar mass
357.1800g/mol
Density
1.6756g/cm3
Appearence

4-(4-Chlorosulfonylphenoxy)benzenesulfonyl chloride appears as a white to pale yellow crystalline powder. The substance is known for its potential to emit toxic fumes of chloride and sulfur dioxide when heated to decomposition. It is normally handled in its solid form, and it should be protected from moisture and sources of ignition.

Comment on solubility

Solubility of 4-(4-chlorosulfonylphenoxy)benzenesulfonyl chloride

The solubility of 4-(4-chlorosulfonylphenoxy)benzenesulfonyl chloride in various solvents is an important characteristic to understand its potential applications. This compound exhibits unique solubility properties due to its molecular structure:

  • Solvent Polarities: It shows varying solubility in polar and non-polar solvents. For instance, it is generally more soluble in polar organic solvents such as dimethyl sulfoxide (DMSO) and acetonitrile.
  • Temperature Dependency: Solubility can increase with temperature, which is a common phenomenon in many chemicals.
  • Hydrophobic Interactions: Given the presence of sulfonyl groups, it may have reduced solubility in highly apolar solvents.
  • Hydrogen Bonding: The sulfonyl groups can participate in hydrogen bonding, which can influence solubility in different environments.

In summary, understanding the solubility of this compound is crucial for its utilization in various chemical reactions and applications. Factors influencing its solubility must be carefully considered, as solubility will greatly affect its reactivity and the effectiveness in end-use situations.

Interesting facts

Interesting Facts about 4-(4-chlorosulfonylphenoxy)benzenesulfonyl chloride

4-(4-chlorosulfonylphenoxy)benzenesulfonyl chloride, often referred to in scientific contexts due to its complex structure, is a fascinating compound due to its versatility and various applications in organic chemistry.

Key Characteristics:

  • Sulfonyl Chloride Group: This compound features a sulfonyl chloride group, known for its reactivity. This makes it a valuable building block in the synthesis of pharmaceuticals and agrochemicals.
  • Functionalized Aromatic Structure: The compound has multiple aromatic rings, which contribute to its stability and play a crucial role in its reactivity. The presence of the chlorosulfonyl group further adds to its functional diversity.

Applications and Uses:

  • Intermediate in Synthesis: It is commonly used as an intermediate in the synthesis of more complex molecules, particularly in the development of drugs.
  • Agrochemical Development: The compound finds application in the formulation of herbicides and pesticides, highlighting its significance in agriculture.
  • Research Tool: In chemical research, it serves as a reagent for various reactions, enabling chemists to modify aromatic compounds effectively.

Exciting Reactions:

This compound can participate in several noteworthy reactions, such as:

  • Nucleophilic Substitution: The sulfonyl chloride can undergo nucleophilic substitution, providing pathways to synthesize diverse sulfonamides.
  • Electrophilic Aromatic Substitution: The presence of the electron-withdrawing groups enhances the reactivity of the aromatic system, making it more susceptible to substitution reactions.

In conclusion, 4-(4-chlorosulfonylphenoxy)benzenesulfonyl chloride exemplifies how complex organic compounds can offer wide-ranging applications across different fields, from pharmaceuticals to agriculture. Its unique structure not only makes it an essential tool for chemists but also serves as an interesting subject for study in the realm of organic synthesis.

Synonyms
121-63-1
4,4'-Bis(chlorosulfonyl)diphenyl ether
Bis(4-chlorosulfonylphenyl) ether
4,4'-OXYBIS(BENZENESULFONYL CHLORIDE)
4,4'-Oxydibenzenesulfonyl chloride
Benzenesulfonyl chloride, 4,4'-oxybis-
Oxybis(4-benzenesulfonyl chloride)
Oxybis(benzenesulfonyl chloride)
4,4'-Oxybenzenesulfonylchloride
Diphenyl ether 4,4'-disulfonyl chloride
Phenoxybenzene-4,4'-disulfonyl chloride
4-(4-chlorosulfonylphenoxy)benzenesulfonyl chloride
p,p'-Oxybis(benzenesulfonyl chloride)
Benzenesulfonyl chloride, 4,4'-oxydi-
HSDB 5591
NSC 212
4,4'-Oxybis(benzene-1-sulphonyl) dichloride
EINECS 204-488-8
D24HP42U4T
DTXSID5059531
NSC-212
4,4/'-Bis(chlorosulfonyl)diphenyl ether
4,4'-Oxybis[benzenesulfonyl chloride]
MFCD00024884
UNII-D24HP42U4T
SCHEMBL433497
4,4'Oxybenzenesulfonylchloride
4-[4-(chlorosulfonyl)phenoxy]benzenesulfonyl chloride
NSC212
Bis(4-chlorosulfonylphenyl)ether
Bis(4chlorosulfonylphenyl) ether
DTXCID0033677
4,4'oxydibenzenesulfonyl chloride
Oxybis(4benzenesulfonyl chloride)
Benzenesulfonyl chloride,4'-oxydi-
Benzenesulfonyl chloride,4'-oxybis-
p,p'Oxybis(benzenesulfonyl chloride)
Benzenesulfonyl chloride, 4,4'oxydi
Benzenesulfonyl chloride, 4,4'oxybis
Phenoxybenzene4,4'disulfonyl chloride
AKOS005139305
4,4-Bis(Chlorosulfonyl)Diphenyl Ether
Diphenyl ether 4,4'disulfonyl chloride
FO62672
4,4'-Bis(chlorosulfonyl)biphenyl ether
4,4\'-Oxybis(benzenesulfonyl Chloride)
DB-041625
4,4'-Oxybis(benzene-1-sulfonyl) dichloride
NS00023971
O0298
D91858