| Weight | 331.132 g/mol |
|---|---|
| Formula | C15H32Sn |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 11 |
Allyltributyltin (24850-33-7)
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- REACTIONS OF ALLYLTIN COMPOUNDS III. ALLYLATION OF AROMATIC HALIDES WITH ALLYLTRIBUTYLTIN IN THE PRESENCE OF TETRAKIS(TRIPHENYLPHOSPHINE)PALLADIUM(O) (Chemistry Letters, 1977)
- Tandem N-AlkylationC-Allylation Reaction of -Imino Esters with Organoaluminums and Allyltributyltin (Journal of the American Chemical Society, 2003)
- A SeCSe-Pd(II) pincer complex as a highly efficient catalyst for allylation of aldehydes with allyltributyltin (Journal of Organic Chemistry, 2006)
- Creation of quaternary stereocenters by the addition of allyltributyltin to chiral cyclic N-acyliminium ions (Tetrahedron-asymmetry, 2000)
- Bis(NHC)-Pd(II) complexes as highly efficient catalysts for allylation of aldehydes with allyltributyltin (Tetrahedron, 2008)
- A Facile Synthesis of 3-Allyl-4-hydrazinocyclopentenes by the Palladium/Lewis Acid Mediated Ring Opening of Bicyclic Hydrazines with Allyltributyltin and Allyltrimethylsilane. (Tetrahedron, 2006)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCCC[Sn](CCCC)(CCCC)CC=C
-
InChIKeyYLGRTLMDMVAFNI-UHFFFAOYSA-N
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Allyltributyltin
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