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2-(Dimethylaminomethyl)ferrocen-1-yl-palladium(II) chloride dinorbornylphosphine complex

Catalog Number
ACM614753514-1
Product Name
2-(Dimethylaminomethyl)ferrocen-1-yl-palladium(II) chloride dinorbornylphosphine complex
Structure
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CAS
614753-51-4
  • Product Overview
  • Usage
Synonyms
Chloro-2-(dimethylaminomethyl)-ferrocen-1-yl-(dinorbornylphosphine)palladium
Molecular Weight
606.3
Molecular Formula
C27H39ClFeNPPd
Canonical SMILES
CN(C)C[C]1[CH][CH][CH][C-]1.C1CC2CC1CC2PC3CC4CCC3C4.[CH]1[CH][CH][CH][CH]1.Cl[Pd+].[Fe]
InChI
InChI=1S/C14H23P.C8H11N.C5H5.ClH.Fe.Pd/c1-3-11-5-9(1)7-13(11)15-14-8-10-2-4-12(14)6-10;1-9(2)7-8-5-3-4-6-8;1-2-4-5-3-1;/h9-15H,1-8H2;3-5H,7H2,1-2H3;1-5H;1H;/q;-1;+2/p-1
InChI Key
ULZLFKCWRWQURL-UHFFFAOYSA-M
Melting Point
155 °C
Purity
97%+
Appearance
Powder
Exact Mass
605.08928
Monoisotopic Mass
605.08928
Rotatable Bond Count
4
Topological Polar Surface Area
3.2 Ų
Application
The 2-(Dimethylaminomethyl)ferrocen-1-yl-palladium(II) chloride dinorbornylphosphine complex serves as an orange powder catalyst renowned for its efficiency in various chemical reactions. Specifically, it is utilized to facilitate the amination of aryl chlorides and the synthesis of substituted biaryl anilines and phenols. Moreover, this catalyst supports the direct vinylation and difluorovinylation of arylboronic acids and plays a crucial role in the Heck coupling of vinyl phosphates. This product is offered through a collaboration with Solvias AG.
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