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ChemicalBook--->CAS DataBase List--->791-28-6

791-28-6

791-28-6 Structure

791-28-6 Structure
IdentificationMore
[Name]

Triphenylphosphine oxide
[CAS]

791-28-6
[Synonyms]

AURORA KA-1603
TPO
TRIPHENYLPHOSPHINE OXIDE
(C6H5)3P=O
Phosphine oxide, triphenyl-
Triphenyl phosphorus oxide
Triphenylphosphanoxid
Triphenylphosphanoxide
triphenyl-phosphineoxid
triphenylphosphorusoxide
TriphenylphosphineOxide,>98%
Triphenylphosphineoxide,99%
TPPO: Triphenylphosphine Oxide
Triphenylphosphinoxid
TPPO
oxo(triphenyl)phosphorane
Di(phenyl)phosphorylbenzene
Triphenylphosphine monoxide
Trisphenylphosphine oxide
[EINECS(EC#)]

212-338-8
[Molecular Formula]

C18H15OP
[MDL Number]

MFCD00002080
[Molecular Weight]

278.28
[MOL File]

791-28-6.mol
Chemical PropertiesBack Directory
[Appearance]

White solid
[Melting point ]

150-157 °C(lit.)
[Boiling point ]

360 °C
[bulk density]

400-450kg/m3
[density ]

1,212 g/cm3
[vapor pressure ]

<1 hPa (50 °C)
[Fp ]

180 °C
[storage temp. ]

Store at RT.
[solubility ]

methanol: 25 mg/mL, clear
[form ]

Crystalline Powder or Flakes
[color ]

White to pink-brown
[Specific Gravity]

1.212
[Water Solubility ]

slightly soluble
[Hydrolytic Sensitivity]

4: no reaction with water under neutral conditions
[BRN ]

745854
[LogP]

2.8
[CAS DataBase Reference]

791-28-6(CAS DataBase Reference)
[NIST Chemistry Reference]

(C6H5)3PO(791-28-6)
[EPA Substance Registry System]

791-28-6(EPA Substance)
Safety DataBack Directory
[Hazard Codes ]

Xn,Xi
[Risk Statements ]

R22:Harmful if swallowed.
R36/37/38:Irritating to eyes, respiratory system and skin .
R52/53:Harmful to aquatic organisms, may cause long-term adverse effects in the aquatic environment .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S61:Avoid release to the environment. Refer to special instructions safety data sheet .
S36:Wear suitable protective clothing .
[RIDADR ]

3077
[WGK Germany ]

2
[RTECS ]

SZ1676000
[Autoignition Temperature]

590 °C
[TSCA ]

Yes
[HazardClass ]

9
[PackingGroup ]

III
[HS Code ]

29310095
[Toxicity]

LD50 orally in Rabbit: 685 mg/kg
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Ethyl diphenylphosphinite-->Diphenylphosphine oxide-->1,3-diisopropylurea-->Benzyltriphenylphosphonium chloride-->TERT-BUTYL (3-IODOPROPYL)CARBAMATE-->3-(BOC-AMINO)-1-PROPANOL-->4-ISOPROPYLBENZYL CHLORIDE
[Preparation Products]

4-Fluorothiophenol-->1-METHYLTHYMINE-->Diethyl acetylenedicarboxylate-->Triphenylphosphine-->2,4,6-TRINITROANILINE-->Phosphine oxide, diethylphenyl--->1-Butamine 4-azide-->beta-D-Glucopyranosylamine-->(METHOXYMETHYL)DIPHENYLPHOSPHINE OXIDE-->Peachflure-->Methyl(triphenyl)phosphonium chloride-->Methyl (3R)-3-(tert-butyldimethylsilyloxy)-5-oxo-6-triphenylphosphoranylidenehexanoate
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

Triphenylphosphine oxide(791-28-6).msds
Hazard InformationBack Directory
[Description]

Triphenylphosphine oxide (TPPO) is a coordinating solvent used to activate crystallization of chemical compounds. It has been used in flame retardant applications, as an epoxy cure catalyst, and more recently, to produce nanostructures.
[Chemical Properties]

White solid
[Uses]

Triphenylphosphine Oxide (Orlistat USP Related Compound C) is a catalyst in the conversion of aldehydes into 1,1-dichlorides. Triphenylphosphine Oxide is used as a catalyst for the synthesis of hightly functionalized α-CF3 γ-keto esters.
[Uses]

Triphenylphosphine oxide can be used:
As a catalyst in Appel-type chlorination reaction of acyclic primary and secondary alcohols.
As a catalyst in stereoselective poly and dibromination of α,β-unsaturated esters and β,γ-unsaturated α-ketoester compounds.
As a promotor in the diastereoselective synthesis of α-ribofuranosides through ribofuranosylation of alcohols with ribofuranosyl iodides.
[Uses]

Triphenylphosphine oxide is a phosphine ligand used for coupling reactions, epoxidations, and Michael reactions
[Definition]

ChEBI: A phosphine oxide in which the substituents on phosphorus are three phenyl groups.
[Synthesis Reference(s)]

Tetrahedron Letters, 31, p. 5463, 1990 DOI: 10.1016/S0040-4039(00)97873-0
[Flammability and Explosibility]

Notclassified
[reaction suitability]

reagent type: ligand
reaction type: Coupling Reactions
reagent type: ligand
reaction type: Epoxidations
reagent type: ligand
reaction type: Michael Reaction
[Purification Methods]

It crystallises from absolute EtOH and is dried in vacuo. The gold chloride complex has m 177.5-178.5o. [Addison & Sheldon J Chem Soc 2705 1956, Cox & Westheimer J Am Chem Soc 80 5441 1958, Beilstein 16 III 864, 16 1011.]
Spectrum DetailBack Directory
[Spectrum Detail]

Triphenylphosphine oxide(791-28-6)MS
Triphenylphosphine oxide(791-28-6)1HNMR
Triphenylphosphine oxide(791-28-6)13CNMR
Triphenylphosphine oxide(791-28-6)IR1
Triphenylphosphine oxide(791-28-6)IR2
Triphenylphosphine oxide(791-28-6)Raman
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

Triphenylphosphine oxide, 99%(791-28-6)
[Alfa Aesar]

Triphenylphosphine oxide, 99%(791-28-6)
[Sigma Aldrich]

791-28-6(sigmaaldrich)
[TCI AMERICA]

Triphenylphosphine Oxide,>98.0%(GC)(791-28-6)
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