tert-Butyldiphenylphosphine, 97%

Code: 591688-5g D2-231

Not available outside of the UK & Ireland.

Application

Catalyst for: Nickel/Lewis acid-catalyzed carbocyanation of alkynes with acetonitrile or substituted acetonitriles Palladium catalyzed hydrocarboxylation of acety...


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$313.66 5G
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Not available outside of the UK & Ireland.

Application

Catalyst for: Nickel/Lewis acid-catalyzed carbocyanation of alkynes with acetonitrile or substituted acetonitriles Palladium catalyzed hydrocarboxylation of acetylene with carbon monoxide to acrylic acid under mild conditions Palladium to form a catalyst for methoxycarbonylation reactions Ru-catalyzed transfer hydrogenation in reductive coupling of disubstituted allenes with aldehydes Stereoselective silylation by dehydrogenative Si-O coupling with Si-stereogenic silanes Phosphine ligand in nickel-catalyzed carbocyanation of alkynes Monodentate P-Donor Ligands (LKB-P)

Packaging

1, 5 g in glass bottle

assay97%
bp144-146 °C/2 mmHg (lit.)
functional groupphosphine
InChI keyQZUPHAGRBBOLTB-UHFFFAOYSA-N
InChI1S/C16H19P/c1-16(2,3)17(14-10-6-4-7-11-14)15-12-8-5-9-13-15/h4-13H,1-3H3
mp52-57 °C (lit.)
Quality Level100
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 stringCC(C)(C)P(c1ccccc1)c2ccccc2
Cas Number6002-34-2
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