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Triethylphosphine information


Triethylphosphine
Names
Preferred IUPAC name
Triethylphosphane
Identifiers
CAS Number
  • 554-70-1
3D model (JSmol)
  • Interactive image
ChEBI
  • CHEBI:39971
ChemSpider
  • 25463
ECHA InfoCard 100.008.245 Edit this at Wikidata
EC Number
  • 209-068-8
Gmelin Reference
2485
PubChem CID
  • 27365
UNII
  • 5W435D16PM
CompTox Dashboard (EPA)
  • DTXSID3060293 Edit this at Wikidata
InChI
  • InChI=1S/C6H15P/c1-4-7(5-2)6-3/h4-6H2,1-3H3
    Key: RXJKFRMDXUJTEX-UHFFFAOYSA-N
SMILES
  • CCP(CC)CC
Properties
Chemical formula
C6H15P
Molar mass 118.160 g·mol−1
Appearance colorless liquid
Density 0.802 g/cm3
Boiling point 127–128 °C (261–262 °F; 400–401 K)
Hazards
GHS labelling:
Pictograms
GHS02: FlammableGHS05: Corrosive
Signal word
Danger
Hazard statements
H224, H225, H250, H314
Precautionary statements
P210, P222, P233, P240, P241, P242, P243, P260, P264, P280, P301+P330+P331, P302+P334, P303+P361+P353, P304+P340, P305+P351+P338, P310, P321, P363, P370+P378, P403+P235, P405, P422, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Triethylphosphine is the organophosphorus compound with the formula P(CH2CH3)3, commonly abbreviated as PEt3. It is a colorless liquid with an unpleasant odor characteristic of alkylphosphines. The compound is a common ligand in organometallic chemistry, such as in auranofin.

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Triethylphosphine

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Triethylphosphine is the organophosphorus compound with the formula P(CH2CH3)3, commonly abbreviated as PEt3. It is a colorless liquid with an unpleasant...

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Phosphine

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compounds containing phosphorus, which he named "trimethylphosphine" and "triethylphosphine", in analogy with "amine" (organo-nitrogen compounds), "arsine" (organo-arsenic...

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Trans effect

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Example of the structural trans effect: the effect induced by triethylphosphine ligands is stronger than induced by chloride ion ligands....

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Elimination reaction

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Allan F.; Whitesides, George M. (1981-02-01). "Ring strain in bis(triethylphosphine)-3,3-dimethylplatinacyclobutane is small". Journal of the American...

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Perkow reaction

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Perkow reaction hexachloroacetone triethylphosphine adduct...

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Trimethylphosphine

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ISBN 0-13-035471-6. T. Yoshida; T. Matsuda; S. Otsuka (1990). "Tetrakis(Triethylphosphine)Platinum(0)". Inorganic Syntheses. Vol. 28. pp. 122–123. doi:10.1002/9780470132593...

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Proton affinity

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Dimethylamine 923 Pyridine 924 Trimethylamine 942 Trimethylphosphine 950 Triethylphosphine 969 Triethylamine 972 Lithium hydroxide 1008 Sodium hydroxide 1038...

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Organocopper chemistry

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complexes can be produced. One such derivative is π-cyclopentadienyl(triethylphosphine)copper(I). Copper halides react with organolithium reagents to give...

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Cobalt compounds

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[Co(NO)2X]2 (X = Cl, Br or I). The complex of cobalt halides and triethylphosphine ((C2H5)3P) can absorb nitric monoxide in benzene to form the diamagnetic...

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Hydrodefluorination

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perfluorinated pyridine reacts with bis(cyclooctadiene)nickel(0) and triethylphosphine to the oxidative addition product and then with HCl to the ortho-hydrodefluorinated...

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List of compounds with carbon number 8

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chloride 111-64-8 C8H15ClO2 hexyl chloroacetate 5927-57-1 C8H15CoNO3P triethylphosphine cobalt dicarbonyl nitrosyl 21485-16-5 C8H15N octahydroindolizine 13618-93-4...

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Transition metal phosphido complexes

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(1987). "Reactions of phosphine, arsine, and stibine with carbonylbis(triethylphosphine)iridium(I) halides. Part 1. Reactions in toluene; X-ray crystal structures...

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Gallium monoiodide

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form Ga(III)I3PPh3. It also reacts with the less sterically hindered triethylphosphine (PEt3) to form a Ga(II)-Ga(I)-Ga(II) mixed valent complex with datively...

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Tetrabromonickelate

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(o-CH3C6H6PEt3)2NiBr4 can be made from the reaction of o-tolyl bis-triethylphosphine, nickel bromide and o-tolyl bromide. (o-CH3OC6H6PEt3)2NiBr4 and (C6H5PEt3)2NiBr4...

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