Skip to Content
Merck
All Photos(4)

Documents

205877

Sigma-Aldrich

Palladium(II) bromide

99%

Synonym(s):

Palladium dibromide, Palladous bromide

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
Br2Pd
CAS Number:
Molecular Weight:
266.23
EC Number:
MDL number:
UNSPSC Code:
12352302
PubChem Substance ID:
NACRES:
NA.23

Assay

99%

form

powder

reaction suitability

reagent type: catalyst
core: palladium

density

5.173 g/mL at 25 °C (lit.)

SMILES string

Br[Pd]Br

InChI

1S/2BrH.Pd/h2*1H;/q;;+2/p-2

InChI key

INIOZDBICVTGEO-UHFFFAOYSA-L

Looking for similar products? Visit Product Comparison Guide

General description

Palladium(II) bromide (PdBr2) is widely used as Pd(II) catalyst. PdBr2 can be prepared by reacting palladium metal with HNO3 and HBr. Electrosynthesis of PdBr2 from palladium metal and HBr has been reported.

Application

Palladium(II) bromide (PdBr2) has been used as a source of Pd(0) precatalyst in various coupling reactions. It was also employed as catalyst for the carbonylative Heck coupling reaction of aryl bromides and vinyl ethers.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Palladium (II) Bromide.
Mahoney SJ, et al.
e-EROS Encyclopedia of Reagents for Organic Synthesis. (2013)
Johannes Schranck et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 18(16), 4827-4831 (2012-03-17)
Three COming together: The first carbonylative Heck coupling reaction of aryl bromides and vinyl ethers leading to 1-aryl-3-alkoxy-2-propen-1-ones has been established (see scheme). Based on this coupling methodology, a novel one-pot synthesis of aryl-substituted pyrazoles was also realized.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service