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Merck
CN

672343

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:
Molecular Weight:
337.44
UNSPSC Code:
12352005
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
9924511
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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

SMILES string

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

InChI key

HDZRDZCQFYUOHE-UHFFFAOYSA-N

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

Quality Level

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

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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Articles

cataCXium® ligands facilitate cross-coupling reactions, essential in polymer science, fine chemicals, and pharmaceutical industries.

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Phosphine Ligand Application Guide

The Catalexis platform enhances catalysis by digitally optimizing catalyst selection to identify the most effective phosphine ligands for cross-coupling reactions.

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