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Triphenylphosphine: Phosphine, triphenyl

This material may be converted directly to a phosphonium salt 1.40 g. (0.0054 mole) of the crude iodide is dissolved in 20 ml. of benzene, and 1.42 g, (0.0054 mole) of triphenylphosphine [Phosphine, triphenyl-] is added. On standing, 2.5 g. (77%) of the triphenylphosphonium salt precipitates as a colorless 1 1 complex with benzene, m.p. 135-137°. Recrystallization from methanol-benzene raises the melting point to 140-142°. Analysis calculated for C28H29PI CeH6 C, 68.23 H, 5.39. Found C, 68.15 H, 5.28. [Pg.81]

Bromo-3-phenylpropane Benzene, (3-bromopropyl)- (8,9) (637-59-2) Triphenylphosphine Phosphine, triphenyl- (8,9) (603-35-0)... [Pg.81]

Trimethyltin chloride Stannane, chlorotrimethyl- (1066-45-1), 68,116 Trimethylvinyltin Stannane, trimethylvinyl- (754-06-3), 68, 116 Triphenylphosphine Phosphine, triphenyl- (603-35-0), 68,130,138 69, 39 Tripropylaluminum (102-67-0), 66, 186, 188, 193 Tris(diethylamino)sulfonium difluorotrimethylsilicate Sulfur (1+), tris(N-ethyl ethanaminato)-, difluorotrimethylsilicate (1-) (59201-86-4), 69, 48, 49 Tris(tetrabutylammonium) hydrogen pyrophosphate trihydrate ... [Pg.164]

See other pages where Triphenylphosphine: Phosphine, triphenyl is mentioned: [Pg.57]    [Pg.47]    [Pg.43]    [Pg.196]    [Pg.146]    [Pg.59]    [Pg.115]    [Pg.328]    [Pg.168]    [Pg.172]    [Pg.190]    [Pg.218]    [Pg.137]    [Pg.147]    [Pg.187]    [Pg.339]    [Pg.9]    [Pg.17]    [Pg.187]    [Pg.339]    [Pg.137]    [Pg.276]    [Pg.104]    [Pg.245]   
See also in sourсe #XX -- [ Pg.33 , Pg.53 , Pg.75 , Pg.155 ]

See also in sourсe #XX -- [ Pg.33 , Pg.53 , Pg.75 , Pg.76 , Pg.155 , Pg.180 ]

See also in sourсe #XX -- [ Pg.33 , Pg.53 , Pg.75 , Pg.155 ]

See also in sourсe #XX -- [ Pg.39 , Pg.68 , Pg.69 , Pg.130 , Pg.138 ]

See also in sourсe #XX -- [ Pg.33 , Pg.53 , Pg.75 , Pg.76 , Pg.155 , Pg.180 ]

See also in sourсe #XX -- [ Pg.33 , Pg.53 , Pg.75 , Pg.76 , Pg.155 , Pg.180 ]



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Phosphine triphenyl

Phosphines triphenylphosphines

Triphenyl

Triphenyls

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