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Naphthalene-1,5-disulfonyl chloride

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Identification
Molecular formula
C10H6Cl2O4S2
CAS number
2459-05-4
IUPAC name
naphthalene-1,5-disulfonyl chloride
State
State

The compound is in a solid state at room temperature, typically presented as crystalline powder.

Melting point (Celsius)
133.00
Melting point (Kelvin)
406.15
Boiling point (Celsius)
305.20
Boiling point (Kelvin)
578.35
General information
Molecular weight
301.19g/mol
Molar mass
301.1930g/mol
Density
1.6600g/cm3
Appearence

Naphthalene-1,5-disulfonyl chloride appears as a white to light-yellow powdered solid. This compound may have a slight characteristic odor.

Comment on solubility

Solubility of Naphthalene-1,5-disulfonyl Chloride

Naphthalene-1,5-disulfonyl chloride, with the chemical formula C10H8ClO2S2, exhibits some intriguing solubility characteristics that are noteworthy for its utilization in various chemical applications. Here are some key points regarding its solubility:

  • Solvent Compatibility: Naphthalene-1,5-disulfonyl chloride is primarily soluble in polar organic solvents such as dimethyl sulfoxide (DMSO) and dichloromethane.
  • Water Solubility: This compound generally shows poor solubility in water due to its bulky aromatic structure and the presence of sulfonyl groups that can hinder aqueous solvation.
  • Temperature Effects: Increased temperature can enhance the solubility of naphthalene-1,5-disulfonyl chloride in organic solvents, making it essential to consider temperature conditions during dissolution.

In applications where this compound is utilized, understanding its solubility is crucial for effective handling and formulation. “A thorough knowledge of solvent interactions with naphthalene-1,5-disulfonyl chloride can lead to better handling techniques and efficient reactions.” Therefore, selecting the right solvent plays a vital role in maximizing its performance in chemical processes.

Interesting facts

Interesting Facts about Naphthalene-1,5-Disulfonyl Chloride

Naphthalene-1,5-disulfonyl chloride is a fascinating compound widely recognized in the realm of organic chemistry for its unique structure and applications. This compound is an aromatic sulfonyl chloride, which means it contains both sulfonyl (–SO2) and chlorine (–Cl) functional groups attached to a naphthalene backbone. Here are some intriguing aspects:

  • Versatile Reactivity: Being a sulfonyl chloride, it readily participates in nucleophilic substitution reactions, making it an essential building block in the synthesis of various organic compounds.
  • Functional Group Transformation: The presence of the sulfonyl group allows for easy transformation into other derivatives, such as sulfonamides, which are crucial for pharmaceutical applications.
  • Color Indicators: Many organic reactions involving naphthalene derivatives change the color of the reaction mixture, making it a useful indicator for chemists during synthesis processes.
  • Keywords in Synthesis: This compound is often mentioned in the synthesis of complex organic molecules, highlighting its importance in the field of medicinal chemistry and materials science.

As Marie Curie once said, "Nothing in life is to be feared, it is only to be understood." The study of compounds like naphthalene-1,5-disulfonyl chloride exemplifies the beauty and complexity of chemical reactions, encouraging scientists to delve deeper into their properties and potential applications.

In conclusion, naphthalene-1,5-disulfonyl chloride is more than just a chemical entity; it serves as a crucial tool for innovation in synthetic chemistry, underlining the importance of understanding how even small changes in molecular structure can lead to significant advancements in science.

Synonyms
1,5-NAPHTHALENEDISULFONYL CHLORIDE
DTXSID20172874
NSC 2022
DTXCID7095365
naphthalene-1,5-disulfonyl chloride
1928-01-4
1,5-Naphthalenedisulfonyl dichloride
SCHEMBL3133065
NSC2022
BCXWMIMRDMIJGL-UHFFFAOYSA-N
NSC-2022