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ALD00608

Sigma-Aldrich

Ni(bpy)3Br2

Synonym(s):

Trisbipyridylnickel dibromide

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About This Item

Empirical Formula (Hill Notation):
C30H24Br2N6Ni
Molecular Weight:
687.05
UNSPSC Code:
12352300

form

powder or crystals

reaction suitability

reagent type: catalyst
reaction type: Cross Couplings

Application

Ni(bpy)3Br2 is a Ni precatalyst shown by the Baran Lab to be an effective catalyst for the electrochemical amination (e-amination) of arly halides with amines.

Product can be used with our Synlectro electrochemistry platform (ESYNTH001)

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pictograms

Health hazardEnvironment

signalword

Danger

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 1B Inhalation - Muta. 2 - Repr. 1B - Resp. Sens. 1B - Skin Sens. 1B - STOT RE 1 Inhalation

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Yu Kawamata et al.
Journal of the American Chemical Society, 141(15), 6392-6402 (2019-03-25)
C-N cross-coupling is one of the most valuable and widespread transformations in organic synthesis. Largely dominated by Pd- and Cu-based catalytic systems, it has proven to be a staple transformation for those in both academia and industry. The current study

Related Content

The Baran Group works with Sigma-Aldrich in providing a portfolio of zinc-based reagents promoting difluoromethylation, trifluoromethylation, trifluoroethylation and isopropylation of aryl and heteroaryl motifs. Baran’s lab has also helped introduce a portable desaturase (Tz0Cl), which promotes the installation of alcohol and amine groups and leaves behind a highly useful tosyl group for further transformations.

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