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
About This Item
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Quality Level
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
Legal Information
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
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cataCXium® ligands facilitate cross-coupling reactions, essential in polymer science, fine chemicals, and pharmaceutical industries.
cataCXium® ligands facilitate cross-coupling reactions, essential in polymer science, fine chemicals, and pharmaceutical industries.
cataCXium® ligands facilitate cross-coupling reactions, essential in polymer science, fine chemicals, and pharmaceutical industries.
cataCXium® ligands facilitate cross-coupling reactions, essential in polymer science, fine chemicals, and pharmaceutical industries.
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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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