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672343

Sigma-Aldrich

2-(Di-tert-butylphosphino)-1-phenylindole

95%

Synonym(s):

N-Phenyl-2-(di-tert-butylphosphino)indole, N-Phenylindol-2-yl-di-tert-butylphosphine, cataCXium® PIntB

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About This Item

Empirical Formula (Hill Notation):
C22H28NP
CAS Number:
740815-37-6
Molecular Weight:
337.44
Beilstein:
9924511
MDL number:
MFCD06798302
UNSPSC Code:
12352005
PubChem Substance ID:
329760468
NACRES:
NA.22

Assay

95%

reaction suitability

reaction type: Asymmetric synthesis
reagent type: ligand
reaction type: Buchwald-Hartwig Cross Coupling Reaction
reagent type: ligand
reaction type: Sonogashira Coupling
reagent type: ligand
reaction type: Suzuki-Miyaura Coupling

functional group

phosphine

SMILES string

CC(C)(C)P(c1cc2ccccc2n1-c3ccccc3)C(C)(C)C

InChI

1S/C22H28NP/c1-21(2,3)24(22(4,5)6)20-16-17-12-10-11-15-19(17)23(20)18-13-8-7-9-14-18/h7-16H,1-6H3

InChI key

HDZRDZCQFYUOHE-UHFFFAOYSA-N

General description

sold in collaboration with Solvias AG

Legal Information

WO 2004/101581
cataCXium is a registered trademark of Umicore AG & Co. KG

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCF5112
BCCC2442
BCBV9294
BCBR3137V
BCBQ6413V

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Articles

cataCXium®

cataCXium® - Ligands and Complexes for Efficient Cross-Coupling Reactions. Cross-coupling reactions are an important class of catalytic transformations with applications in polymer science as well as in the fine chemicals and pharmaceutical industries.

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