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

ʻO ka wehewehe pōkole:

Inoa: Tris(dibenzylideneacetone)dipalladium(0)

Nā huaʻōlelo like: Pd2(dba)3;Tris(dba)dipalladium(0)

CAS: 51364-51-3

ʻIke: >97.0%

Pd: 20.9~21.9%

Nānā: Pada ʻEleʻele

E-Mail: alvin@ruifuchem.com


Huahana Huahana

Nā Huahana Pili

Huahana Huahana

wehewehe:

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

Na Waiwai Kemika:

Inoa Kimia Tris(dibenzylideneacetone)dipalladium(0)
Nā huaʻōlelo like [Pd2(dba)3] x dba;Pd2dba3;Pd2(dba)3;Tris(dba)dipalladium(0);Bis[tris(dibenzylideneacetone)palladium(0)]
Helu CAS 51364-51-3
Helu CAT RF-PI2210
Kūlana Kūʻai Loaʻa
ʻĀpana Molekala C51H42O3Pd2
Kaumaha Molecular 915.73
Lae hehee 152.0~155.0 ℃
Pilikino Māmā Māmā, Kūleʻa Ea, Māmā
Hiki i ka wai ʻAʻole hiki ke hoʻonā i ka wai
Brand Kemika Ruifu

Nā kikoʻī:

'ikamu Nā kikoʻī
Ka nana aku Pauda ʻeleʻele ʻeleʻele
Hoʻāʻo >97.0%
Maʻiʻo Palladium (Pd) 20.9~21.9% (ICP)
Kalapona ma ka Elemental Analysis 64.6~69.2%
Huina metalaka paumaele ≤1600ppm
He mea haumia hoʻokahi ≤100ppm
Infrared Spectrum Kūlike i ka hoʻolālā
Proton NMR Spectrum Kūlike i ka hoʻolālā
Kūlana hoʻāʻo Kūlana ʻoihana
Ola Pahu 24 mahina

Pūʻolo a me ka waiho ʻana:

Pūʻolo: ʻO ka ʻōmole, pahu, a i ʻole e like me ka makemake o ka mea kūʻai aku

Kūlana mālama:E mālama i loko o nā pahu i hoʻopaʻa ʻia ma kahi maloʻo a maloʻo;E pale i ka malamalama a me ka wai

Pono:

1

FAQ:

Noi:

ʻO Tris(dibenzylideneacetone)dipalladium(0), synonyms Pd2(dba)3, (CAS: 51364-51-3) he cycloaddition catalyst, ʻo ia ka Pd0 precursor complex i hoʻohana nui ʻia i ka synthesis a me ka catalysis, ma ke ʻano he catalyst no nā ʻano like ʻole. hoʻopili ʻana i nā hopena.Hoʻohana ʻia ia ma ke ʻano he catalyst no nā ʻano like ʻole o ka Pd catalyzed reactions me Suzuki coupling, Heck coupling, Negishi coupling, Carroll reaarangement, Trost asymmetric allylic alkylation, Buchwald-Hartwig amination of acryl halides, fluorination of allylic chlorides, arylation of ketones, carbonylation of ketones. 1,1-dichloro-1-alkenes, ß-arylation o na esters carboxylic, a me ka hoohuli ana i ka aryl a me ka vinyl triflates i aryl a me vinyl halides.Hoʻopili pū ia i ka synthesis o azepane.Hoʻohana ʻia ʻo Tris(dibenzylideneacetone)dipalladium(0) i ka hoʻomākaukau ʻana i nā polymers semiconducting i hana ʻia mai nā solvents nonchlorinated i loko o nā transistors kiʻiʻoniʻoni lahilahi.Hoʻohana pū ʻia i ka synthesis o ka polymer bulk-heterojunction solar kūʻai aku ma ke ʻano he semiconductor.ʻO kāna hana e pili ana i ke kumu metala, Asymmetric synthesis, Catalysis a catalyst, Coupling reactions, Cross couplings, Heck Reaction, Ligands, Organic synthesis, Suzuki coupling, Polymer science, Materials Chemistry, Column chromatography and Organic Compounds, and Arylations, Aminations, Deprotonations , Hydroxylations, Fluorinations.Catalyst precursor no ka hoohuli ana o aryl chlorides, triflates, a nonaflates i nitroaromatics.Catalyst no ka synthesis o epoxides.Catalytic asymmetric allylic a me ka homoallylic diamination o nā olefins hope.Site-koho i benzylic sp3 palladium-catalyzed pololei arylation.Palladium-catalyzed one-pot synthesis o tricyclic indolines.Hoʻoikaika ikaika no ka hui ʻana o Suzuki-Miyaura o nā nucleophiles 2-pyridyl.Catalyst i hui pū me BINAP no ka asymmetric Heck Arylation o nā olefins.Precursor for palladium-catalyzed carbon-nitrigen bond formation.Catalyst no ka α-arylation o na ketones.ʻO ka hui ʻana o nā aryl halides me nā waikawa aryl boronic.

E kākau i kāu leka ma aneʻi a hoʻouna mai iā mākou