Triphenylphosphine, ReagentPlus, 99%

Code: T84409-1G D2-231

Application

Triphenylphosphine was used in the synthesis of mono-6-amino-deoxy-6-cyclodextrin. It was also employed as catalyst during the synthesis of C-aryl furanosides.

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Your Price
£14.00 1G
£16.80 inc. VAT

Application

Triphenylphosphine was used in the synthesis of mono-6-amino-deoxy-6-cyclodextrin. It was also employed as catalyst during the synthesis of C-aryl furanosides.

General description

Rhodium and triphenylphosphine catalyst system has been used for the hydroformylation of soybean, safflower and linseed oils and their methyl esters. Polymer supported triphenylphosphine has been reported to efficiently catalyze the γ-addition of pronucleophiles to alkynoate. Triphenylphosphine reacts with hydrated ruthenium trichloride in methanol to afford [RuCl2(PPh3)4], [RuCl2(PPh3)3] and [RuCl3(PPh3)2CH3OH]. It participates in the Heck reaction of 4-bromoanisole and ethyl acrylate in ionic liquids.

Legal Information

ReagentPlus is a registered trademark of Sigma-Aldrich Co. LLC

Packaging

10 kg in poly drum

1 kg in poly bottle

1, 25, 100, 500 g in poly bottle

assay99%
bp377 °C (lit.)
functional groupphosphine
InChI keyRIOQSEWOXXDEQQ-UHFFFAOYSA-N
InChI1S/C18H15P/c1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15H
mp79-81 °C (lit.)
product lineReagentPlus®
Quality Level200
reaction suitabilityreaction type: Buchwald-Hartwig Cross Coupling Reaction, reaction type: Hiyama Coupling, reaction type: Heck Reaction, reaction type: Sonogashira Coupling, reaction type: Suzuki-Miyaura Coupling, reaction type: Negishi Coupling, reaction type: Stille Coupling, reagent type: ligandreaction type: Cross Couplings
SMILES stringc1ccc(cc1)P(c2ccccc2)c3ccccc3
vapor density9 (vs air)
vapor pressure5 mmHg ( 20 °C)
Code
Description
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T84409-100G
Unit:100G
List Price: £46.30
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T84409-1KG
Unit:1KG
List Price: £154.00
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T84409-25G
Unit:25G
List Price: £26.30
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T84409-500G
Unit:500G
List Price: £119.00
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Cas Number603-35-0
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