2-(Trimethylsilyl)ethanol
2-(Trimethylsilyl)ethanol structure
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Common Name | 2-(Trimethylsilyl)ethanol | ||
|---|---|---|---|---|
| CAS Number | 2916-68-9 | Molecular Weight | 118.250 | |
| Density | 0.825 | Boiling Point | 145.0±13.0 °C at 760 mmHg | |
| Molecular Formula | C5H14OSi | Melting Point | 0ºC | |
| MSDS | USA | Flash Point | 50.6±0.0 °C | |
| Symbol |
GHS02 |
Signal Word | Warning | |
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Effects of charge, volume, and surface on binding of inhibitor and substrate moieties to acetylcholinesterase.
J. Med. Chem. 28(9) , 1309-13, (1985) Reversible inhibitors for acetylcholinesterase, AcChE, have been studied. Sterically similar alcohols with tetra-substituted uncharged beta groups, (CH3)3SiCH2CH2OH (I), (CH3)3CCH2CH2OH (IA), and CH3S(O2)CH2CH2OH (VII), bind similarly, KI = 3-9 mM, and each b... |
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Generation of aza-ortho-xylylenes via ring opening of 2-(2-acylaminophenyl)aziridines: application in the construction of the communesin ring system.
Org. Lett. 8 , 3995, (2006) A new protocol for generating aza-ortho-xylylenes via acid-catalyzed or fluoride-promoted ring opening of 2-(2-acylaminophenyl)aziridines is described. This methodology has been exploited in the rapid construction of a hexacyclic substructure of communesin B. |
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Silicon compounds as substrates and inhibitors of acetylcholinesterase.
Biochim. Biophys. Acta 791(2) , 278-80, (1984) Several trimethylsilyl derivatives were found to be ligands of acetylcholinesterase (acetylcholine acetylhydrolase, EC 3.1.1.7): trimethylsilylethyl acetate (III) and trimethylsilylmethyl acetate (V) are substrates of the enzyme, whereas trimethylsilylethanol... |
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J. Chem. Soc. Perkin Trans. I , 2639, (1993)
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J. Org. Chem. 59 , 6687, (1994)
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Tetrahedron Lett. 35 , 757, (1994)
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Tetrahedron Lett. 33 , 7685, (1992)
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Synlett , 2670, (2006)
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