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4,6-Bis(diphenylphosphino)phenoxazine, min. 98% NIXANTPHOS|15-0437|261733-18-0

4,6-Bis(diphenylphosphino)phenoxazine, min. 98% NIXANTPHOS

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Sku SC15-0437_2_G
US-Strem
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Product Information

Product Name
4,6-Bis(diphenylphosphino)phenoxazine, min. 98% NIXANTPHOS
Brand Name
US-Strem
Product Number
15-0437
CAS
261733-18-0
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
3255346
IUPAC Name
(6-diphenylphosphanyl-10H-phenoxazin-4-yl)-diphenylphosphane
InChI Key
HSWZLYXRAOXOLL-UHFFFAOYSA-N
SMILES
C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=CC=CC4=C3OC5=C(N4)C=CC=C5P(C6=CC=CC=C6)C7=CC=CC=C7

Description

Technical Note： 1. A large bite angle chelating bisphosphine that provides high levels of linear-to branched selectivity in the hydroformylation of
alkenes .
2.A Deprotonatable L igand for Room-Temperature Palladium-Catalyzed Cross-Couplings of Aryl Chlorides.
References:
1.Organometallics. 2000, 19, 872.
2.J. Am. Chem. Soc.. 2014, 136, 6276.

References Data Source From Pubchem

Highly Efficient and Linear-Selective Hydroformylation of Allyl Acetate Under Mild Conditions Regulated by Additives
Publication Name: Catalysis Letters
Publication Date: 2024-06-03
DOI: 10.1007/s10562-024-04720-z

Features of Polymerization of Methyl Methacrylate in the Presence of New Ruthenium(II) and Ruthenium(III) Carborane Complexes with Chelate P‒O‒P Ligands
Publication Name: Polymer Science, Series B
Publication Date: 2024-02
DOI: 10.1134/s1560090424600219

Alkoxycarbonylation of Unsaturated Substrates of Plant Origin in the Presence of Palladium Catalysts as a Route to Synthesize Ester Products
Publication Name: Catalysis in Industry
Publication Date: 2023-12
DOI: 10.1134/s2070050423040104

Recent Advances in Decarboxylative Conversions of Cyclic Carbonates and Beyond
Publication Name: Synthesis
Publication Date: 2022-02-15
DOI: 10.1055/a-1715-7413

Palladium-Catalyzed Benzylic C(sp3)–H Carbonylative Arylation of Azaarylmethyl Amines
Publication Name: Synfacts
Publication Date: 2021-09-17
DOI: 10.1055/s-0040-1720224