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Benzeneselenol information


Benzeneselenol
Names
IUPAC name
Benzeneselenol
Other names
  • Phenylselenol
  • Selenaphenol
  • Selenophenol
Identifiers
CAS Number
  • 645-96-5 checkY
3D model (JSmol)
  • Interactive image
ChemSpider
  • 62734 checkY
ECHA InfoCard 100.010.417 Edit this at Wikidata
EC Number
  • 211-457-2
PubChem CID
  • 69530
CompTox Dashboard (EPA)
  • DTXSID30275709 Edit this at Wikidata
InChI
  • InChI=1S/C6H6Se/c7-6-4-2-1-3-5-6/h1-5,7H checkY
    Key: WDODWFPDZYSKIA-UHFFFAOYSA-N checkY
  • InChI=1/C6H6Se/c7-6-4-2-1-3-5-6/h1-5,7H
    Key: WDODWFPDZYSKIA-UHFFFAOYAD
SMILES
  • [SeH]c1ccccc1
Properties
Chemical formula
C6H5SeH
Molar mass 157.085 g·mol−1
Appearance colorless liquid
Odor extremely foul yet characteristic
Density 1.479 g/cm3
Boiling point 71 to 72 °C (160 to 162 °F; 344 to 345 K) (18 mmHg)
Solubility in water
slightly
Solubility in other solvents most organic solvents
Refractive index (nD)
1.616
Structure
Dipole moment
1.1 D
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
toxic
GHS labelling:
Pictograms
GHS06: ToxicGHS08: Health hazardGHS09: Environmental hazard
Signal word
Danger
Hazard statements
H301, H331, H373, H410
Related compounds
Related compounds
  • Phenol
  • Thiophenol
  • Hydrogen selenide
  • Diphenyl diselenide
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)
Infobox references

Benzeneselenol, also known as selenophenol, is the organoselenium compound with the chemical formula C6H5SeH, often abbreviated PhSeH. It is the selenium analog of phenol. This colourless, malodorous compound is a reagent in organic synthesis.[1]

  1. ^ Cite error: The named reference eEROS was invoked but never defined (see the help page).

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Benzeneselenol

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Benzeneselenol, also known as selenophenol, is the organoselenium compound with the chemical formula C6H5SeH, often abbreviated PhSeH. It is the selenium...

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Diphenyl diselenide

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abbreviated Ph2Se2. This yellow-coloured solid is the oxidized derivative of benzeneselenol. It is used as a source of the PhSe unit in organic synthesis. Ph2Se2...

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Selenonic acid

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for phenyl) is a white solid. It can be prepared by the oxidation of benzeneselenol. Selenenic acid Seleninic acid IUPAC, Compendium of Chemical Terminology...

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Selenium

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selenols include respectively selenomethionine, diphenyldiselenide, and benzeneselenol. The sulfoxide in sulfur chemistry is represented in selenium chemistry...

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Thiophenol

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thiols 1,2-Benzenedithiol Benzenemethanethiol Related compounds Phenol Benzeneselenol Diphenyl disulfide Except where otherwise noted, data are given for...

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Selenol

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organolithium reagents or Grignard reagents with elemental Se. For example, benzeneselenol is generated by the reaction of phenylmagnesium bromide with selenium...

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Organoselenium chemistry

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compounds are relatively unstable and generally have an unpleasant smell. Benzeneselenol (also called selenophenol or PhSeH) is more acidic (pKa 5.9) than thiophenol...

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List of compounds with carbon number 6

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tricarballylic anhydride 500000-19-1 C6H6S benzenethiol 108-98-5 C6H6Se benzeneselenol 645-96-5 C6H6V benzenevanadium 61332-91-0 C6H7 methylcyclopentadienyl...

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Selenium compounds

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selenols include respectively selenomethionine, diphenyldiselenide, and benzeneselenol. The sulfoxide in sulfur chemistry is represented in selenium chemistry...

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