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Tetraallylsilane

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For Research Use Only | Not For Clinical Use
CATAP1112669
CAS1112-66-9
Structure
MDL NumberMFCD00048161
Molecular Weight192.37
InChI KeyAKRQMTFHUVDMIL-UHFFFAOYSA-N
REAXYS Number1750943
Description≥97.0% (GC)
Density0.831 g/mL at 25 °C (lit.)
Assay≥97.0% (GC)
BP90 °C/3 mmHg (lit.)
Linear Formula(H2C=CHCH2)4Si
Refractive Indexn20/D 1.485 (lit.); n20/D 1.485
Size5ML
1

"A Posteriori" Modification of Carbosilane Dendrimers and Dendrons: Their Activation in Core and Branch Positions

Arno Tuchbreiter, Helmut Werner, Lutz H Gade

Dalton Trans. 2005 Apr 21;(8):1394-402.

PMID: 15824777

1

Cu(OTf) 2-Catalyzed Pummerer Coupling of β-Ketosulfoxides

Regev Parnes, Hagai Reiss, Doron Pappo

J Org Chem. 2018 Jan 19;83(2):723-732.

PMID: 29293340

1

The First Catalytic Asymmetric Allylation of Imines With the tetraallylsilane-TBAF-MeOH System, Using the Chiral Bis-Pi-Allylpalladium Complex

Rodney A Fernandes, Yoshinori Yamamoto

J Org Chem. 2004 Feb 6;69(3):735-8.

PMID: 14750798

1

Transition-metal-promoted Reactions of Boron Hydrides. 17. Titanium-catalyzed Decaborane-Olefin Hydroborations

M J Pender, P J Carroll, L G Sneddon

J Am Chem Soc. 2001 Dec 12;123(49):12222-31.

PMID: 11734022

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