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Merck
CN

92877

1,4-Bis(diphenylphosphino)butane-palladium(II) chloride

≥95.0%, powder

Synonym(s):

Dichloro-1,4-bis(diphenylphosphino)butane-palladium(II), Palladium(II) chloride 1,4-bis(diphenylphosphino)butane complex, PdCl2(dppb)

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About This Item

Empirical Formula (Hill Notation):
C28H28Cl2P2Pd
CAS Number:
Molecular Weight:
603.80
UNSPSC Code:
12352300
PubChem Substance ID:
NACRES:
NA.22
MDL number:
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Product Name

1,4-Bis(diphenylphosphino)butane-palladium(II) chloride, ≥95.0%

SMILES string

Cl[Pd]Cl.C(CCP(c1ccccc1)c2ccccc2)CP(c3ccccc3)c4ccccc4

InChI key

JQXJBXVWVPVTOO-UHFFFAOYSA-L

InChI

1S/C28H28P2.2ClH.Pd/c1-5-15-25(16-6-1)29(26-17-7-2-8-18-26)23-13-14-24-30(27-19-9-3-10-20-27)28-21-11-4-12-22-28;;;/h1-12,15-22H,13-14,23-24H2;2*1H;/q;;;+2/p-2

assay

≥95.0%

form

powder

reaction suitability

core: palladium, reaction type: Buchwald-Hartwig Cross Coupling Reaction, reaction type: Cross Couplings, reaction type: Heck Reaction, reaction type: Hiyama Coupling, reaction type: Negishi Coupling, reaction type: Sonogashira Coupling, reaction type: Stille Coupling, reaction type: Suzuki-Miyaura Coupling, reagent type: catalyst

Application

catalyst for coupling reactions

Other Notes

Palladium-catalyzed cross-coupling and coupling reactions

Storage Class

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

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MethCohn, O.; Jiang, H.
Journal of the Chemical Society. Perkin Transactions 1, 3737-3737 (1998)
Minato, K.; Suzuki, K et al.
Journal of the Chemical Society. Chemical Communications, 511-511 (1984)
Bjork, P.; Hornfeldt, A.-B. et al.
Journal of Heterocyclic Chemistry, 31, 1161-1161 (1994)
M. Kranenburg et al.
European Journal of Inorganic Chemistry, 155-155 (1998)
Kentaro Masui et al.
Journal of the American Chemical Society, 126(16), 5074-5075 (2004-04-22)
Palladium-catalyzed C-H homocoupling of thiophene derivatives takes place in the presence of silver(I) fluoride or acetate. A variety of bithiophenes are obtained in good to excellent yields. In particular, the reaction of 2-bromothiophene proceeds at room temperature to afford 5,5'-dibromo-2,2'-bithiophene

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