913278
[1,2-Bis(diphenylphosphino)ethane]dibromonickel(II)
≥95%
Synonym(s):
dppeNiBr2
About This Item
Recommended Products
Assay
≥95%
form
powder
reaction suitability
reagent type: catalyst
reaction type: Cross Couplings
mp
322-326 °C
InChI
1S/C26H24P2.2BrH.Ni/c1-5-13-23(14-6-1)27(24-15-7-2-8-16-24)21-22-28(25-17-9-3-10-18-25)26-19-11-4-12-20-26;;;/h1-20H,21-22H2;2*1H;/q;;;+2/p-2
InChI key
AEGMSHMBRVOLMV-UHFFFAOYSA-L
Application
- kumada catalyst-transfer polycondensation
- oxidation of carboranyl phosphine ligands
- synthesis of nickel-iron dithiolato hydrides
- hydroformylation of alcohols
- Ullmann reactions - homocoupling reactions
- intramolecular aerobic oxidative amination of alkenes
related product
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 1A Inhalation - Muta. 2 - Repr. 1B - Resp. Sens. 1 - Skin Sens. 1 - STOT RE 1
Storage Class Code
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
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Articles
Nickel complexes catalyze various synthetic reactions like oxidative addition, C-H activation, and cross-coupling.
Nickel complexes catalyze various synthetic reactions like oxidative addition, C-H activation, and cross-coupling.
Nickel complexes catalyze various synthetic reactions like oxidative addition, C-H activation, and cross-coupling.
Nickel complexes catalyze various synthetic reactions like oxidative addition, C-H activation, and cross-coupling.
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