Tris(dibenzylideneacetone)dipalladium(0) CAS 51364-51-3 Intende >97.0% Pd 20.9~21.9%

Description:

Nomen: Tris (dibenzylideneacetone) dipalladium(0)

Synonyma: Pd2(dba)3;Tris(dba)dipalladium(0)

CAS: 51364-51-3

Dic: >97.0%

Pd: 20.9~21.9%

Aspectus: Niger pulveris

E-Mail: alvin@ruifuchem.com

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Product Detail

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Descriptio:

Shanghai Ruifu Chemical Co., Ltd. is the leading manufacturer of Tris(dibenzylideneacetone)dipalladium(0) (CAS: 51364-51-3) with high quality. We can provide COA, worldwide delivery, small and bulk quantities available. Please contact: alvin@ruifuchem.com

Chemical Properties:

Nomen chemicum	Tris(dibenzylideneacetone)dipalladium(0)
Synonyma	[Pd2(dba)3] x dba;Pd2dba3;Pd2(dba)3;Tris(dba)dipalladium(0);Bis[tris(dibenzylideneacetone)palladium(0)]
CAS Number	51364-51-3
CATTUS Number	RF-PI2210
Stock Status	In Stock
Formulae hypotheticae	C51H42O3Pd2
M. Pondus	915.73
Liquescens punctum	152.0~155.0℃
Sensitiva	Lux Sensitiva, Aeris Sensitiva, umor Sensitiva
Aqua Solubility	Insolubilis in aqua
Brand	Ruifu Chemical

Specifications:

Item	Specifications
Aspectus	Nigrum Purpura pulveris
Assay	>97.0%
Palladium Content (Pd)	20.9~21.9% (ICP)
Carbon by Elemental Analysis	64.6~69.2%
Totalis immunditias metallicis	≤1600ppm
Unius immunditiae Content	≤100ppm
Infrared Imaginis	Conformat ut Structure
Proton NMR Spectrum	Conformat ut Structure
Test Standard	Enterprise Standard
Fasciae vita	XXIV Menses

Sarcina & Repono:

sarcina: Utrem, Drum, vel secundum exigentiam emptoris

Repono Condition:Repone in vasis signatis in loco frigido et sicco;Protege a lumine et humore

commoda:

FAQ:

Applicatio:

Tris(dibenzylideneacetone)dipalladium(0), synonyma Pd2(dba)3, (CAS: 51364-51-3) catalysta cycloadditio est, quam latissime Pd0 praecursor complexus est in synthesi et catalysi, praesertim catalysta pro variis. copulatio profectae.Adhibetur catalysta pro varietate Pd catalysis reactiones inter Suzuki copulationem, Heck copulatio, Negishi copulatio, Carroll rearangementum, Trost asymmetrica alkylationis allicui, Buchwald-Hartwig aminatio halidum acryl, fluorinationis chloridum alliicarum, arylationum ketonum, carbonylationum 1,1-dichloro-1-alkenes, ß-arylationum esters carboxylicorum, et conversio aryl et vinyl triflates ad halides aryl et vinyl.Involvitur etiam in synthesi azepane.Tris (dibenzylideneacetone) dipalladium (0) adhibetur in praeparatione polymerorum semiconducting processit e solventibus nonchlorinatis in altum peractivum cinematographicum transistorum.Etiam usus est in synthesi polymeris mole-heterojunctionis solaris sicut semiconductoris vendit.Eius opera ad metalla deducenda fundamentum, synthesis asymmetrica, catalysis vel catalysta, motus coniunctionis, iuncturae crucis, Heck Reactio, Ligandes, synthesis organica, Suzuki copulatio, scientia polymerica, materia Chemia, columnae chromatographiae et compositiones organicae, Arylationes, Aminationes, Deprotonationes. , Hydroxylations, Fluorinationes.Praecursor catalystus ad conversionem chloridum aryl, triflates et nonaflates ad nitroaromaticas.Catalyst pro synthesi epoxidum.Catalyticum asymmetricum allicum et diaminatum homoallylicum olefinum terminalium.Site-selective benzylic sp3 palladium-catalyzed direct arylation.Palladii catalyses una-olla synthesis tricyclicae indolorum.Activum catalyst pro Suzuki-Miyaura copulatio 2-pyridorum nucleophilorum.Catalyst in compositione cum BINAP pro asymmetrica Heck Arylatione olefins.Praecursor ad palladium-catalyticum vinculi carbonis nitrigeni formatio.Catalyst for α-arylation of ketonum.Crux-coniunctio halidum aryl cum acida aryl boronicis.