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Phenyl Selenohypochlorite

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Identification
Molecular formula
C6H5SeCl
CAS number
69932-80-7
IUPAC name
phenyl selenohypochlorite
State
State

At room temperature, phenyl selenohypochlorite is typically found in a liquid state. It should be stored under appropriate conditions to prevent decomposition and ensure stability.

Melting point (Celsius)
22.50
Melting point (Kelvin)
295.65
Boiling point (Celsius)
142.00
Boiling point (Kelvin)
415.15
General information
Molecular weight
173.54g/mol
Molar mass
173.5400g/mol
Density
2.7450g/cm3
Appearence

Phenyl selenohypochlorite appears as a pale yellow or yellow-green liquid. It may sometimes be observed as a yellowish crystalline substance depending on its state and purification.

Comment on solubility

Solubility of Phenyl Selenohypochlorite

Pheyl selenohypochlorite, with the chemical formula C6H5SeOCl, exhibits unique solubility characteristics that can significantly impact its applications in various chemical processes. Here are some notable points regarding its solubility:

  • Solvent Compatibility: Phenyl selenohypochlorite is generally soluble in organic solvents such as ethanol and chloroform, but is poorly soluble in water.
  • Polarity Influence: Its solubility can be influenced by the polarity of the solvent; polar solvents may struggle to dissolve this compound effectively.
  • Temperature Effects: Like many chemical substances, the solubility of phenyl selenohypochlorite can increase with temperature, making it more useful in certain chemical reactions under heated conditions.
  • Chemical Stability: In highly polar or protic solvents, the compound may undergo hydrolysis, leading to decreased solubility and loss of its integrity.

In application, understanding these solubility trends is vital for utilizing phenyl selenohypochlorite effectively, especially in synthetic organic chemistry where solvent choice can greatly influence reaction pathways and outcomes. As stated, "A good solvent makes a good reaction." Therefore, careful selection based on solubility ensures better performance in practical applications.

Interesting facts

Interesting Facts About Phenyl Selenohypochlorite

Pheyl selenohypochlorite is a fascinating chemical compound that combines elements of both selenium and chlorine. This compound is known for its interesting reactivity and serves as a useful reagent in various chemical syntheses. Here are some intriguing aspects that highlight its significance:

  • Unique Element Pairing: The presence of selenium in phenyl selenohypochlorite gives it distinctive properties that are not found in more common hypochlorite compounds. Selenium, often overlooked, plays a vital role in biological systems and has interesting photochemical properties.
  • Reactivity: As a hypochlorite compound, it acts as a potent oxidizing agent. This makes it valuable in organic synthesis, where selective oxidation is necessary. Its ability to participate in various reaction pathways opens up avenues for innovative chemical transformations.
  • Biological Significance: While there's ongoing research into organoselenium compounds, phenyl selenohypochlorite may offer insights into selenium's role in biological processes. Its reactive nature could be explored for potential applications in medicinal chemistry.
  • Environmental Considerations: Selenium compounds can have both beneficial and detrimental effects in environmental contexts. Understanding their chemistry, including that of phenyl selenohypochlorite, is crucial for developing strategies to manage selenium in ecosystems.
  • Laboratory Applications: This compound can also be used in laboratory settings, particularly in studies involving radical reactions and other complex chemical interactions, showcasing the diversity of chemical methodologies.

The study of phenyl selenohypochlorite and similar compounds not only enriches our understanding of organic chemistry but can also lead to novel applications across various scientific fields. As one researcher aptly stated, "The discovery of new chemical compounds often paves the way for innovation and transformative breakthroughs." Thus, exploring the intricacies of phenyl selenohypochlorite is both exciting and essential to furthering chemical knowledge.

Synonyms
Phenylselenyl chloride
Benzeneselenenyl chloride
Chloroselenobenzene
EINECS 227-196-2
DTXSID00205679
DTXCID80128170
227-196-2
5707-04-0
Phenylselenenyl chloride
phenyl selenohypochlorite
Benzeneselenyl chloride
(phenylselanyl)chlorane
PhSeCl
MFCD00000478
CHEMBL3335712
Phenylselenium chloride
Chlorophenylselenium; Phenylselenium chloride; Phenylselenium monochloride; Phenylselenyl chloride
phenylselenenylchloride
chloroselanylbenzene
Selenium compound 2
phenylselanyl chloride
phenyl selenium chloride
phenyl selenenyl chloride
SCHEMBL29416
Phenylselenyl chloride, 98%
WJCXADMLESSGRI-UHFFFAOYSA-
selenohypochlorous acid phenyl ester
BDBM50028968
AKOS015840367
FP61162
SY009957
CS-0017812
NS00081865
P1091
D78353
EN300-131834
A831301
Z1255485131
InChI=1/C6H5ClSe/c7-8-6-4-2-1-3-5-6/h1-5H