Ethanol,2-(methylsulfonyl)-
Ethanol,2-(methylsulfonyl)- structure
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Common Name | Ethanol,2-(methylsulfonyl)- | ||
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| CAS Number | 15205-66-0 | Molecular Weight | 124.15900 | |
| Density | 1.33 | Boiling Point | 148-149 °C(lit.) | |
| Molecular Formula | C3H8O3S | Melting Point | 31-33 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | >230 °F | |
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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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Mild conversion of electron deficient aryl fluorides to phenols using 2-(methylsulfonyl) ethanol. Rogers JF and Green DF.
Tetrahedron Lett. 43(19) , 3585-87, (2002)
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Reagent effects on distribution of methylsulfonylethyl substituents in the D-glucopyranosyl unit of cotton cellulose. Rowland SP, et al.
Can. J. Chem. 46(3) , 451-7, (1968)
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Sulfonyl-containing aldophosphamide analogues as novel anticancer prodrugs targeted against cyclophosphamide-resistant tumor cell lines.
J. Med. Chem. 47(15) , 3843-52, (2004) A series of sulfonyl-group containing analogues of aldophosphamide (Aldo) were synthesized as potential anticancer prodrugs that liberate the cytotoxic phosphoramide mustards (PM, IPM, and tetrakis-PM) via beta-elimination, a nonenzymatic activation mechanism... |