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900287

PCy3 Pd G4

95%, powder

Sustainability features

Sinónimos:

(methanesulfonato-κO)[2′-(methylamino-κN)[1,1′-biphenyl]-2-yl-κC](tricyclohexylphosphine)-palladium

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Talla/SKUDisponibilidadPrecio
250 mg
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87,80 €
1 g
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275,00 €
5 g
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810,00 €

Acerca de este artículo

Fórmula empírica (notación de Hill):
C32H48NO3PPdS
Número CAS:
Peso molecular:
664.19
MDL number:
UNSPSC Code:
12161600
PubChem Substance ID:
NACRES:
NA.22

87,80 €


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Nombre del producto

PCy3 Pd G4,

Quality Segment

product line

Buchwald precatalyst Generation 4

assay

95%

form

powder

feature

generation 4

reaction suitability

reaction type: Buchwald-Hartwig Cross Coupling Reaction, 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
reaction type: Cross Couplings

greener alternative product characteristics

Catalysis
Learn more about the Principles of Green Chemistry.

sustainability

Sustainability features, Sustainability features

mp

214-219 °C

functional group

phosphine

greener alternative category

SMILES string

C[NH+]1C2=C(C3=C([Pd-2]1([P+](C4CCCCC4)(C5CCCCC5)C6CCCCC6)OS(C)(=O)=O)C=CC=C3)C=CC=C2

InChI

1S/C18H33P.C13H12N.CH4O3S.Pd/c1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;1-14-13-10-6-5-9-12(13)11-7-3-2-4-8-11;1-5(2,3)4;/h16-18H,1-15H2;2-7,9-10,14H,1H3;1H3,(H,2,3,4);/q;;;+1/p-1

InChI key

VGKOWIXQRLSMGH-UHFFFAOYSA-M

General description

We are committed to providing greener alternatives that adhere to the 12 Principles of Green Chemistry. This catalyst enables efficient catalytic transformations aligned with green chemistry principles, promoting atom economy, waste reduction and catalysis. Click here for more information.

Application

A powerful ligand for classic cross-coupling reactions combined with the Buchwald Fourth Generation Palladacycle. Bench stable, soluble in most organic solvents.

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Este artículo
764175900620900284
description

-

description

97%

description

-

description

-

reaction suitability

reaction type: Stille Coupling, reaction type: Hiyama Coupling, reaction type: Heck Reaction, reaction type: Suzuki-Miyaura Coupling, reaction type: Buchwald-Hartwig Cross Coupling Reaction, reagent type: catalyst
reaction type: Cross Couplings, reaction type: Sonogashira Coupling, reaction type: Negishi Coupling

reaction suitability

reaction type: Suzuki-Miyaura Coupling, reaction type: Sonogashira Coupling, reaction type: Heck Reaction, reaction type: Stille Coupling, reagent type: catalyst
reaction type: Cross Couplings, reaction type: Negishi Coupling, reaction type: Hiyama Coupling, reaction type: Buchwald-Hartwig Cross Coupling Reaction

reaction suitability

reaction type: Negishi Coupling, reagent type: catalyst
reaction type: Cross Couplings, reaction type: Sonogashira Coupling, reaction type: Hiyama Coupling, reaction type: Stille Coupling, reaction type: Heck Reaction, reaction type: Buchwald-Hartwig Cross Coupling Reaction, reaction type: Suzuki-Miyaura Coupling

reaction suitability

reaction type: Buchwald-Hartwig Cross Coupling Reaction, reaction type: Hiyama Coupling, reaction type: Sonogashira Coupling, reaction type: Stille Coupling, reaction type: Suzuki-Miyaura Coupling, reagent type: catalyst
reaction type: Cross Couplings, reaction type: Heck Reaction, reaction type: Negishi Coupling

assay

95%

assay

97%

assay

-

assay

-

functional group

phosphine

functional group

phosphine

functional group

phosphine

functional group

phosphine

form

powder

form

solid

form

powder

form

powder

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

mp

214-219 °C

mp

219-224 °C (decomposition)

mp

-

mp

-


Clase de almacenamiento

11 - Combustible Solids



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