| Weight | 172.3 g/mol |
|---|---|
| Formula | C8H16O2Si |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 4 |
54125-02-9 (59414-23-2, 54125-02-9)
1-methoxy-3-trimethylsilyloxy-1,3-butadiene
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- Diels-Alder reactions of trans-1-methoxy-3-trimethylsilyloxy-1,3-butadiene (Journal of the American Chemical Society, 1979)
- Derivatives of 1-methoxy-3-trimethylsilyloxy-1,3-butadiene for Diels-Alder reactions (Journal of the American Chemical Society, 1979)
- On the conversion of 1-glutamate to 1-dopa : The preparation and chemistry of 1-methoxy-2-acetoxy-3-trimethylsilyloxy-1,3-butadiene (Tetrahedron, 1981)
- Synthesis of chromones and 4-hydroxyquinolines based on uncatalyzed condensations of 1-methoxy-1,3-bis(trimethylsilyloxy)-1,3-butadiene with 2-alkoxy- and 2-nitrobenzoyl chlorides and related reactions (Organic and Biomolecular Chemistry, 2009)
- A synthesis of oxygenated 1-azaanthraquinones via Diels-Alder reaction of 2,4-dioxygenated quinoline-5,8-diones with 1-methoxy-3-trimethylsilyloxy-1,3-butadiene (Heterocycles, 2002)
- Stereoselective synthesis of new -lactams by cyclocondensation of 1-methoxy-3-(trimethylsilyloxy)-1,3-butadiene with 4-formyl substituted azetidinones (Farmaco, 1998)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 1-methoxy-3-trimethylsilyloxy-1,3-butadiene
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SMILESCOC=CC(=C)O[Si](C)(C)C
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InChIKeySHALBPKEGDBVKK-UHFFFAOYSA-N
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Synthesis
Reactant
+
Chlorotrimethylsilane
(Alcohol protection with TMSCl)
Reactant
+
CHLOROMETHYL METHYL ETHER
(Wittig)
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54125-02-9
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