Di-chlorobis[(1,2,3-)-1-phenyl-2-propenyl]dipalladium(II)

Di-chlorobis[(1,2,3-)-1-phenyl-2-propenyl]dipalladium(II) Basic information
Application Reaction
Product Name:Di-chlorobis[(1,2,3-)-1-phenyl-2-propenyl]dipalladium(II)
Synonyms:Di-chlorobis[(1,2,3-)-1-phenyl-2-propenyl]dipalladium(II), 98%;Di-μ-chlorobis[(1,2,3-η)-1-phenyl-2-propenyl]dipalladiuM(II),98%;Cinnamylpalladium chloride dimer;PalladiuM(II)(pi-cinnaMyl) Chloride DiMer;PalladiuM(II)(π-cinnaMyl) Chloride DiMer;PalladiuM(pi-cinnaMyl) chloride diMer 97%;Di-μ-chlorobis[(1,2,3-η)-1-phenyl-2-propenyl]dipalladium(Ⅱ);Di-μ-chlorobis[(1,2,3-η)-1-phenyl-2-propen-1-yl]dipalladium
CAS:12131-44-1
MF:C18H12Cl2Pd2
MW:512.03
EINECS:234-579-8
Product Categories:Pd
Mol File:12131-44-1.mol
Di-chlorobis[(1,2,3-)-1-phenyl-2-propenyl]dipalladium(II) Structure
Di-chlorobis[(1,2,3-)-1-phenyl-2-propenyl]dipalladium(II) Chemical Properties
Melting point 218-220°C
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
form crystal
color yellow
Sensitive air sensitive
Safety Information
Hazard Codes T
Risk Statements 23-43
Safety Statements 36/37-45
RIDADR UN 2811 6.1 / PGIII
WGK Germany 3
HS Code 2843909000
MSDS Information
Di-chlorobis[(1,2,3-)-1-phenyl-2-propenyl]dipalladium(II) Usage And Synthesis
Application

Di-chlorobis[(1,2,3-)-1-phenyl-2-propenyl]dipalladium(ii) is an important organic regant for the use of transition-metal-mediated organic syntheses. It can be used as a catalyst for the ammonia cross-coupling reactions to synthesize arylamines and conversion of aryl triflates to fluorides.

Reaction
  1. Precursor for the preparation of a palladium catalyst used in the carbonylative arylation of ketones, yielding vinylbenzoate compounds.
  2. Precursor for the preparation of a palladium catalyst used in the Buchwald-Hartwig amination of (hetero)aryl chlorides.
  3. Precursor for the preparation of a palladium catalyst used in the arylative dearomatization of phenols.
  4. Versatile palladium precursor for the preparation of palladium catalysts used in the cross-coupling of aryl chlorides and amines , conversion of aryl triflates to aryl fluorides , and the α-arylation of aldehydes .
Reactions of 12131-44-1
UsesPalladium(π-cinnamyl) chloride dimer can be used as a catalyst for the:
  • Ammonia cross-coupling reactions to synthesize arylamines.
  • Conversion of aryl triflates to fluorides.

It can also be used as a source of palladium in the asymmetric α-arylation of amides.
Di-chlorobis[(1,2,3-)-1-phenyl-2-propenyl]dipalladium(II) Preparation Products And Raw materials
Nickel chloride METHOXYCARBONYLSULFENYL CHLORIDE Platinum dioxide polymer Dichloro[(±)BINAP]digold(I),97% HYDROXY(1,5-CYCLOOCTADIENE)RHODIUM(I)DIMER Bismuth trichloride Lanthanum(III) chloride Calcium chloride Benzeneruthenium(II) chloride dimer Sodium chloride Allylpalladium(II) Chloride Dimer Lithium chloride monohydrate Zinc chloride DICHLORO[(R)-(+)-2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BINAPHTHYL][(1R,2R)-(+)-1,2-DIPHENYLETHYLENEDIAMINE]RUTHENIUM (II) (T-4)-Dichloro[(oxydi-2,1-phenylene)bis[diphenylphosphine]]nickel CERIUM(III) CHLORIDE HEPTAHYDRATE CROTYLPALLADIUM CHLORIDE DIMER

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