Tris (dibenzylideneacetone) dipalladium (0) CAS 51364-51-3 Kev ntsuam xyuas > 97.0% Pd 20.9 ~ 21.9%
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
Tshuaj npe | Tris (dibenzylideneacetone) dipalladium (0) |
Synonyms | [Pd2(dba)3] x dba;Pd2dba3;Pd2(dba)3;Tris(dba)dipalladium(0);Bis [tris(dibenzylideneacetone)palladium(0)] |
CAS Nr | 51364-51-3 |
CAT Number | Tus Qauv Zauv: RF-PI2210 |
Tshuag xwm txheej | Hauv Tshuag |
Molecular Formula | C51H42O3Pd2 |
Molecular Luj | 915.73 ib |
Melting Point | 152.0 ~ 155.0 ℃ |
rhiab heev | Lub teeb Sensitive, Cua rhiab heev, Moisture Sensitive |
Dej Solubility | Insoluble hauv dej |
Hom | Ruifu Tshuaj |
Yam khoom | Specifications |
Qhov tshwm sim | Dub Ntshav Hmoov |
Assay | > 97.0% |
Palladium Cov ntsiab lus (Pd) | 20.9 ~ 21.9% (ICP) |
Carbon los ntawm Elemental Analysis | 64.6 ~ 69.2% |
Tag nrho cov hlau tsis huv | ≤1600ppm |
Ib Cov ntsiab lus Impurity ib leeg | ≤100ppm |
Infrared Spectrum | Raws li tus qauv |
Proton NMR Spectrum | Raws li tus qauv |
Test Standard | Enterprise Standard |
Txee lub neej | 24 Lub Hlis |
Pob: Lub raj mis, Nruas, lossis raws li cov neeg siv khoom xav tau
Cia txias:Khaws rau hauv cov thawv ntim khoom ntawm qhov chaw txias thiab qhuav;Tiv thaiv los ntawm lub teeb thiab noo noo
Tris(dibenzylideneacetone)dipalladium(0), synonyms Pd2(dba)3, (CAS: 51364-51-3) yog cycloaddition catalyst, yog cov feem ntau siv Pd0 precursor complex hauv synthesis thiab catalysis, tshwj xeeb tshaj yog cov catalyst rau ntau yam kev sib txuas lus.Nws yog siv los ua catalyst rau ntau yam Pd catalyzed cov tshuaj tiv thaiv xws li Suzuki coupling, Heck coupling, Negishi coupling, Carroll rearangement, Trost asymmetric allylic alkylation, Buchwald-Hartwig amination ntawm acryl halides, fluorination ntawm allylic carbon chlorides ntawm ketones, 1,1-dichloro-1-alkenes, ß-arylation ntawm carboxylic esters, thiab hloov pauv ntawm aryl thiab vinyl triflates rau aryl thiab vinyl halides.Nws kuj tseem koom nrog hauv kev sib txuas ntawm azepane.Tris (dibenzylideneacetone) dipalladium (0) yog siv rau hauv kev npaj ntawm semiconducting polymers ua los ntawm nonchlorinated cov kuab tshuaj mus rau hauv kev ua tau zoo nyias zaj duab xis transistors.Kuj tseem siv nyob rau hauv kev sib txuas ntawm polymer bulk-heterojunction hnub ci muag raws li ib qho semiconductor.Nws ua haujlwm ntsig txog cov kab hlau hauv qab, Asymmetric synthesis, Catalysis lossis catalyst, Coupling reactions, Cross couplings, Heck Reaction, Ligands, Organic synthesis, Suzuki coupling, Polymer science, Materials Chemistry, Kem chromatography thiab Organic Compounds, thiab Arylations, Amination, , Hydroxylations, Fluorinations.Catalyst precursor rau kev hloov pauv ntawm aryl chlorides, triflates, thiab nonaflates rau nitroaromatics.Catalyst rau synthesis ntawm epoxides.Catalytic asymmetric allylic thiab homoallylic diamination ntawm terminal olefins.Site-xaiv benzylic sp3 palladium-catalyzed ncaj arylation.Palladium-catalyzed ib lub lauj kaub synthesis ntawm tricyclic indolines.Active catalyst rau Suzuki-Miyaura coupling ntawm 2-pyridyl nucleophiles.Catalyst ua ke nrog BINAP rau asymmetric Heck Arylation ntawm olefins.Precursor rau palladium-catalyzed carbon-nitrigen daim ntawv cog lus.Catalyst rau α-arylation ntawm ketones.Hla-coupling ntawm aryl halides nrog aryl boronic acids.