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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

Quality Level

100

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

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Certificates of Analysis (COA)

Lot/Batch Number
BCCL7905
BCCJ5218
BCCH9223
BCCH6297
BCCC8211

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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
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
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
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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