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Merck
CN

331708

Dibromobis(triphenylphosphine)nickel(II)

99%

Synonym(s):

NiBr2(PPh3)2, bis(triphenylphosphine)nickel(II) bromide

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About This Item

Linear Formula:
[(C6H5)3P]2NiBr2
CAS Number:
Molecular Weight:
743.07
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12161600
MDL number:
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Quality Level

assay

99%

reaction suitability

core: nickel, reagent type: catalyst

mp

219-223 °C (lit.)

SMILES string

Br[Ni]Br.c1ccc(cc1)P(c2ccccc2)c3ccccc3.c4ccc(cc4)P(c5ccccc5)c6ccccc6

InChI

1S/2C18H15P.2BrH.Ni/c2*1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;;;/h2*1-15H;2*1H;/q;;;;+2/p-2

InChI key

QEKXARSPUFVXIX-UHFFFAOYSA-L

Application

Catalysts for the cross-coupling reactions, C-X bond reduction, homocoupling of Csp2 halides, displacement of aryl halides, and oligomerization of dienes


pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves



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Articles

Nickel complexes catalyze various synthetic reactions like oxidative addition, C-H activation, and cross-coupling.


Ho, K. M.; Lam, C. H.; Luh, T.-Y.
The Journal of Organic Chemistry, 54, 4474-4474 (1989)
Takagi, K.; Sakakibara, Y.
Chemistry Letters (Jpn), 1957-1957 (1989)
Kalinin, V. N.
Synthesis, 413-413 (1992)



Global Trade Item Number

SKUGTIN
331708-10G04061826728390
331708-50G04061833546703