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672661

Sigma-Aldrich

2-(Di-tert-butyl-phosphino)-1-phenyl-1H-pyrrole

95%

Synonym(s):

N-Phenyl-2-(di-tert-butylphosphino)pyrrole, N-Phenylpyrrol-2-yldi-tert-butylphosphine, cataCXium® PtB, phosphine ligands

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About This Item

Empirical Formula (Hill Notation):
C18H26NP
CAS Number:
672937-61-0
Molecular Weight:
287.38
Beilstein:
9626114
MDL number:
MFCD05861612
UNSPSC Code:
12352005
PubChem Substance ID:
329760523
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: Dehydrogenation
reagent type: ligand
reaction type: Suzuki-Miyaura Coupling

functional group

phosphine

SMILES string

CC(C)(C)P(c1cccn1-c2ccccc2)C(C)(C)C

InChI

1S/C18H26NP/c1-17(2,3)20(18(4,5)6)16-13-10-14-19(16)15-11-8-7-9-12-15/h7-14H,1-6H3

InChI key

DVVDGSKDQGMLPW-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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Hai T Dong et al.
Inorganic chemistry, 59(20), 14967-14982 (2020-09-30)
We previously reported the synthesis and preliminary characterization of a unique series of low-spin (ls) {FeNO}8-10 complexes supported by an ambiphilic trisphosphineborane ligand, [Fe(TPB)(NO)]+/0/-. Herein, we use advanced spectroscopic techniques and density functional theory (DFT) calculations to extract detailed information
Cen Tang et al.
ACS nano, 14(9), 11605-11612 (2020-09-01)
The capping reagent plays an essential role in the functional properties of gold nanoparticles (AuNPs). Multiple stimuli-responsive materials are generated via diverse surface modification. The ability of the organic ligand shell on a gold surface to create a porous shell
Michelle Muñoz-Osses et al.
Dalton transactions (Cambridge, England : 2003), 47(39), 13861-13869 (2018-09-19)
Cyrhetrenyl aldehyde derivatives [(η5-C5H4CHO)Re(CO)2PR3] with R = methyl (Me, 2a), phenyl (Ph, 2b), and cyclohexyl (Cy, 2c) were synthesized by a photochemical reaction from the starting material [(η5-C5H4CHO)Re(CO)3] (1) and the corresponding phosphines. The complexes were fully characterized by FT-IR
Xun Pan et al.
Dalton transactions (Cambridge, England : 2003), 49(42), 14941-14950 (2020-10-21)
The synthesis of four heteroleptic dinuclear Cu(i) complexes bearing tetraphosphine and diimine ligands was reported. Complexes 1-3 were successfully obtained through microwave synthesis while complex 4 was synthesized through traditionally stirring at room temperature. These complexes are listed as follows:
Xi Kang et al.
Chemical Society reviews, 49(17), 6443-6514 (2020-08-08)
Metal nanoclusters fill the gap between discrete atoms and plasmonic nanoparticles, providing unique opportunities for investigating the quantum effects and precise structure-property correlations at the atomic level. As a versatile strategy, alloying can largely improve the physicochemical performances compared to
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cataCXium® Catalysts

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

cataCXium® Catalysts

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

cataCXium® Catalysts

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

cataCXium® Catalysts

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

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