CAS NO.5518-52-5 Tri(2-furyl)phosphine Basic information | |
Product Name | Tri(2-furyl)phosphine |
Synonyms | SALOR-INT L308749-1EA;TRIS(2-FURYL)PHOSPHINE;TRI(2-FURYL)PHOSPHINE;Tri(2-furyl)phosphine,97%;Tri-2-furylphosphine,98+%;TRI-(2-FURYL)PHOSPHINE 98%;2,2',2''-Phosphinidynetrisfuran;Tri(2-furanyl)phosphine |
Structure |
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CAS NO | 5518-52-5 |
Appearance | white to light yellow crystal powde |
Assay | 98% |
MF: | C12H9O3P |
MW | 232.17 |
EINECS | 1312995-182-4 |
Product Categories | Ligand;Phosphine Ligands;Synthetic Organic Chemistry;Catalysis and Inorganic Chemistry;Phosphine Ligands;Phosphorus Compounds;organophosphorus ligand;Aromatics;Chelating Agents & Ligands;Heterocycles;Achiral Phosphine;Aryl Phosphine |
Storage | Shading, sealed, dry place. |
Capacity | 10000KG /month |
Package | In paper drums /Fluoride drums /iron drums /plastic drums/IBC Tank ,etc. |
Shipment method | By Sea ,Air ,Courier door to door ,etc. |
Loading Port | China any port ,Beijing ,Shanghai ,Hong Kong etc. |
Application | A phopshine ligand used in transition-metal mediated organic synthesis, in particular in wittig reactions to improved (Z) selectivity. |
Organophosphorus Compounds
Diphosphines, sometimes called bisphosphanes, are organophosphorus compounds used as ligands in inorganic and organometallic chemistry. They are identified by the presence of two phosphino groups linked by a backbone, and are usually chelating.
Introduction of CAS NO.5518-52-5 Tri(2-furyl)phosphine
The cores of many types of polymers, ligands, natural products, and pharmaceuticals contain biaryl or substituted aromatic structures, and efficient methods of synthesizing these structures are crucial to the work of a broad spectrum of organic chemists. Recently, Pd-catalyzed carbon-carbon bond-forming processes have risen in popularity for this purpose.new bulky and electron-rich phosphine ligands, which can dramatically improve the efficiency and selectivity of such cross-coupling reactions, have beenintroduced.These ligands can be used for a wide variety of palladium-catalyzed carbon-carbon, carbon-nitrogen, and carbon-oxygen bond-forming processes as well as serving as supporting ligands for a number of other reactions.
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