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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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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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