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54314-85-1 Structure

54314-85-1 Structure
IdentificationBack Directory
[Name]

(3-BENZYLOXYPROPYL)TRIPHENYLPHOSPHONIUM BROMIDE
[CAS]

54314-85-1
[Synonyms]

3-benzyloxypropyl(triphenyl)phosphonium
triphenyl(3-phenylmethoxypropyl)phosphanium
(3-BENZYLOXYPROPYL)TRIPHENYLPHOSPHONIUM BROMIDE
(3-Benzyloxypropyl)triphenylphosphonium bromide 98%
triphenyl(3-phenylmethoxypropyl)phosphanium,bromide
(3-Benzyloxypropyl)triphenylphosphonium bromide, 97+% white to off-white powder
[Molecular Formula]

C28H28BrOP
[MDL Number]

MFCD00191781
[MOL File]

54314-85-1.mol
[Molecular Weight]

491.4
Chemical PropertiesBack Directory
[Melting point ]

153-154 °C(lit.)
[form ]

Powder
[color ]

White to off-white
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P264-P271-P280-P302+P352-P305+P351+P338
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36
[WGK Germany ]

3
[HS Code ]

2931599090
Hazard InformationBack Directory
[Uses]

(3-Benzyloxypropyl)triphenylphosphonium Bromide is a reagent used in the preparation of antitumor and Her2 degradation activity of geldanamycin and radicicol macrocyclic chimeras.
[Uses]

Reactant for preparation of:
  • Spirocyclohexadienones via Pd-catalyzed intramolecular ipso-Friedel-Crafts allylic alkylation
  • Inhibitors of heat shock protein (Hsp90) as antitumor agents
  • Carpanone-like molecules via an oxidative coupling/Diels-Alder cycloaddition sequence
[reaction suitability]

reaction type: C-C Bond Formation
Spectrum DetailBack Directory
[Spectrum Detail]

(3-BENZYLOXYPROPYL)TRIPHENYLPHOSPHONIUM BROMIDE(54314-85-1)IR
(3-BENZYLOXYPROPYL)TRIPHENYLPHOSPHONIUM BROMIDE(54314-85-1)Raman
(3-BENZYLOXYPROPYL)TRIPHENYLPHOSPHONIUM BROMIDE(54314-85-1)FT-IR
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