| Weight | 317.105 g/mol |
|---|---|
| Formula | C14H30Sn |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 10 |
Tributyl(vinyl)tin (7486-35-3)
ethynyltributylstannane · ethynyltributyltin
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- ETHYNYLTRIBUTYLTIN - A SYNTHETIC EQUIVALENT FOR ACETYLENE, ARYL, ACYL AND HALOGENO ALKYNES IN 4+2 CYCLOADDITIONS (Tetrahedron Letters, 1998)
- Synthesis of 3,5-disubstituted pyridazines by regioselective [4+2] cycloadditions with ethynyltributyltin and subsequent replacement of the organotin substituent (Tetrahedron, 1998)
- The dechlorination of poly(vinyl chloride) by zinc and tributyl tin hydride.: Characterization of the product microstructures by carbon-13 NMR (European Polymer Journal, 1982)
- Enol triflates derived from the Wieland-Miescher ketone and an analog bearing an angular acetoxymethyl group : their highly regioselective synthesis and stille coupling with vinyl(tributyl)tin (Tetrahedron Letters, 2006)
- ChemInform Abstract: Ethynyltributyltin A Synthetic Equivalent for Acetylene, Aryl, Acyl, and Halogeno Alkynes in [4 + 2] Cycloadditions. (ChemInform, 2010)
- ChemInform Abstract: Synthesis of 3,5-Disubstituted Pyridazines by Regioselective [4 + 2] Cycloadditions with Ethynyltributyltin and Subsequent Replacement of the Organotin Substituent. (ChemInform, 2010)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - ethynyltributylstannane
- ethynyltributyltin
-
SMILESCCCC[Sn](CCCC)(CCCC)C=C
-
InChIKeyQIWRFOJWQSSRJZ-UHFFFAOYSA-N
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Similar Compounds
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Tributyl(vinyl)tin
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