Tri-tert-butylphosphine tetrafluoroborate

$ 1.00 /1KG

career henan chemical co

7YR

China

Chemical Properties

Product Name	Tri-tert-butylphosphine tetrafluoroborate
CAS No	131274-22-1
EC-No
Min. Order	1G
Purity	99%
Supply Ability	1MT
Release date	2019/07/06

AD68

Tri-tert-butylphosphine tetrafluoroborate Basic information

Reaction

Product Name:	Tri-tert-butylphosphine tetrafluoroborate
Synonyms:	Tri-t-butylphosphoniumtetrafluoroborate,99%;fluoroboric acid tri-tert-butylphosphine adduct;tri-tert-butylphosphine fluoroboric acid adduct;Tri-tert-butylphosphonium tetrafluoroborate, 97+%;Tri-tert-butylphosphonium tetrafluoroborate,99%;Tri-tert-butylphosphoniuM tetrafluoroborate, 97+% 1GR;Tri-tert-butylphosphine tetrafluoborate;Tri-tert-butylphosphoniuM tetr
CAS:	131274-22-1
MF:	C12H28P.BF4
MW:	290.13
EINECS:	-0
Product Categories:	Ligand;Basic Phosphine LigandsCatalysis and Inorganic Chemistry;Catalysis and Inorganic Chemistry;Cross-Coupling;Phosphine Ligands;Phosphorus Compounds;organometallic complex;Organophosphine salt;Achiral Phosphine;Alkyl Phosphine;P-BF4
Mol File:	131274-22-1.mol

Tri-tert-butylphosphine tetrafluoroborate Chemical Properties

Melting point	261 °C(lit.)
form	Crystals and Chunks
color	White
Water Solubility	Soluble in methylene chloride and chloroform. Slightly soluble in terahydro furan. Insoluble in hexane, toluene and water.
Sensitive	Hygroscopic
BRN	8813613
InChIKey	YSTLBJVHZMEEAC-UHFFFAOYSA-N
CAS DataBase Reference	131274-22-1(CAS DataBase Reference)

Safety Information

Tri-tert-butylphosphine tetrafluoroborate Usage And Synthesis

Reaction	Air-stable, non-pyrophoric precursor of the Tri-t-butylphosphine ligand which is used in a variety of catalytic processes. Ligand for Suzuki cross-couplings. Ligand for Heck Reactions. Ligand for Stille Cross-couplings. Ligand for α-Arylation and vinylation of arylmandelic acid derivatives. Ligand for direct arylation of hetercycles Synthesis of benzocyclobutenes by C-H activation. Cross-coupling of Grignard reagents and aryl bromides. Palladium catalyzed annulation of haloanilines. Palladium-Catalyzed Acylation. Palladium Catalyzed Carbonylative Heck Reaction. Palladium-catalyzed aminosulfonylation. Palladium-catalyzed intramolecular C–O bond formation. Ruthenium-catalyzed cross-coupling of aldehydes with arylboronic acid.
Chemical Properties	white to light yellow crystal powde
Uses	suzuki reaction

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