Skip to Content
MilliporeSigma

Key Documents

View All Documentation

741248

Bis(triphenylphosphine)palladium(II) dichloride

solid

Synonym(s):

Dichlorobis(triphenylphosphine)palladium(II), Palladium(II)bis(triphenylphosphine) dichloride, PdCl2(PPh3)2

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

About This Item

Linear Formula:
[(C6H5)3P]2PdCl2
CAS Number:
13965-03-2
Molecular Weight:
701.90
NACRES:
NA.22
PubChem Substance ID:
329765477
UNSPSC Code:
12161600
EC Number:
237-744-2
MDL number:
MFCD00009593
Beilstein/REAXYS Number:
4935975
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

Bis(triphenylphosphine)palladium(II) dichloride,

form

solid

Quality Level

100

reaction suitability

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
core: palladium, reagent type: ligand

functional group

phosphine

SMILES string

Cl[Pd]Cl.c1(P(c2ccccc2)c3ccccc3)ccccc1.c4(P(c5ccccc5)c6ccccc6)ccccc4

InChI

1S/2C18H15P.2ClH.Pd/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

YNHIGQDRGKUECZ-UHFFFAOYSA-L

Application

Bis(triphenylphosphine)palladium(II) dichloride is generally used as a catalyst for the synthesis of conjugated polymers via Stille coupling. It is also applicable to other coupling reactions such as Suzuki- and Sonogashira-coupling reactions
Application Guide for Palladium Catalyzed Cross-Coupling Reactions

Still not finding the right product?

Explore all of our products under Bis(triphenylphosphine)palladium(II) dichloride

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H317,H413

Hazard Classifications

Aquatic Chronic 4 - Skin Sens. 1A

Storage Class

11 - Combustible Solids

flash_point_f

Not applicable

flash_point_c

Not applicable

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

It looks like we've run into a problem, but you can still download Certificates of Analysis from our Documents section.

If you need assistance, please contact Customer Support

Already Own This Product?

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

Visit the Document Library

Synthesis of quaternized zinc (II) and cobalt (II) phthalocyanines bearing pyridine-2-yl-ethynyl groups and their DNA binding properties.
Alishah MM, et al.
Turkish Journal of Chemistry, 42(2), 572-585 (2018)
Influence of catalytic systems in Stille polymerization on the electrochromic performance of diketopyrrolopyrrole-based conjugated polymers.
Neo WT, et al.
Materials Chemistry Frontiers. (2018)
New oligomeric poly (ether-imide) s containing diphenylsilane and dibenzofuran moieties. Synthesis and characterization.
Tundidor-Camba A, et al.
Journal of Macromolecular Science, Part A: Pure and Applied Chemistry, 55(4), 324-331 (2018)
View All Related Papers

Global Trade Item Number

SKUGTIN
741248-1G04061832884516
741248-25G04061832884523
741248-5G04061832884530