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- Bis[(trimethylsilyl)methyl](1,5-cyclooctadiene)palladium(II), 98%
Bis[(trimethylsilyl)methyl](1,5-cyclooctadiene)palladium(II), 98%
PRICE INQUIRYCatalog Number
ACM225931806-1
Product Name
Bis[(trimethylsilyl)methyl](1,5-cyclooctadiene)palladium(II), 98%
Structure
![{[CurrentData.Name]}](https://resource.alfachemic.com/structure/225931-80-6.gif)
CAS
225931-80-6
Synonyms
(1,5-Cyclooctadiene)bis(trimethylsilylmethyl)palladium(II);225931-80-6;
IUPAC Name
(1Z,5Z)-cycloocta-1,5-diene;methanidyl(trimethyl)silane;palladium(2+);
Molecular Weight
389.038g/mol
Molecular Formula
C16H34PdSi2;
Canonical SMILES
C[Si](C)(C)[CH2-].C[Si](C)(C)[CH2-].C1CC=CCCC=C1.[Pd+2];
InChI
InChI=1S/C8H12.2C4H11Si.Pd/c1-2-4-6-8-7-5-3-1;2*1-5(2,3)4;/h1-2,7-8H,3-6H2;2*1H2,2-4H3;/q;2*-1;+2/b2-1-,8-7-;;;;
InChI Key
MEMCDCLCEZMOBR-PHFPKPIQSA-N;
Complexity
140
Covalently-Bonded Unit Count
4
Defined Bond Stereocenter Count
2
Exact Mass
388.123g/mol
H-Bond Acceptor
2
Heavy Atom Count
19
Monoisotopic Mass
388.123g/mol
Topological Polar Surface Area
0A^2
Application
Bis[(trimethylsilyl)methyl](1,5-cyclooctadiene)palladium(II), 98%, serves as a novel palladium complex designed to facilitate the synthesis of allylsilanes through the Silyl-Heck reaction, as well as the formation of aryl fluorides. This innovative product plays a crucial role in advancing methodologies that allow for efficient and selective transformations essential in various chemical synthesis applications.
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