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Merck
CN

763020

[1-(Diphenylphosphino)ethyl]ferrocene

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About This Item

Empirical Formula (Hill Notation):
C24H23FeP
CAS Number:
178388-23-3
Molecular Weight:
398.26
UNSPSC Code:
12352300
PubChem Substance ID:
329767020
MDL number:
MFCD22417227

Key Documents

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InChI

1S/C19H18P.C5H5.Fe/c1-16(17-10-8-9-11-17)20(18-12-4-2-5-13-18)19-14-6-3-7-15-19;1-2-4-5-3-1;/h2-16H,1H3;1-5H;

SMILES string

[Fe].[CH]1[CH][CH][CH][CH]1.CC([C]2[CH][CH][CH][CH]2)P(c3ccccc3)c4ccccc4

InChI key

WNHZFUIMWGWGNB-UHFFFAOYSA-N

form

solid

reaction suitability

core: palladium, 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: Coupling Reactions

pictograms

Health hazardExclamation mark
GHS08,GHS07

signalword

Warning

Hazard Classifications

Repr. 2 - Skin Irrit. 2

Storage Class

4.2 - Pyrophoric and self-heating hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
SHBC3110

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Ping He et al.
Organic letters, 9(2), 343-346 (2007-01-16)
Anionic four-electron donor-based palladacycle-catalyzed 1,4-additions of arylboronic acids with alpha,beta-unsaturated ketones and 1,2-additions of arylboronic acids with aldehydes and alpha-ketoesters are described. Our study demonstrated that palladacycles were highly efficient, practical catalysts for these addition reactions. The work described here

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