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About This Item
线性分子式:
CH3SO2CH2CH2OH
CAS号:
分子量:
124.16
Beilstein:
1746915
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
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方案
98%
沸点
148-149 °C (lit.)
mp
31-33 °C (lit.)
SMILES字符串
CS(=O)(=O)CCO
InChI
1S/C3H8O3S/c1-7(5,6)3-2-4/h4H,2-3H2,1H3
InChI key
KFTYFTKODBWKOU-UHFFFAOYSA-N
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一般描述
Reaction of 2-(methylsulfonyl)ethanol with cotton cellulose yields methylsulfonylethyl substituents in the 2-O- to 6-O-positions of the monosubstituted D-glucopyranosyl unit of cotton cellulose.
应用
2-(Methylsulfonyl)ethanol may be used as reagent in the synthesis of phenols from aryl fluorides. It may be used in the preparation of 2-(methylsulfonyl)ethyl N,N-bis(2-chloroethyl)phosphorodiamidate.
警示用语：
Warning
危险声明
危险分类
Skin Sens. 1
储存分类代码
10 - Combustible liquids
WGK
WGK 3
闪点(°F)
235.4 °F - closed cup
闪点(°C)
113.00 °C - closed cup
个人防护装备
Eyeshields, Gloves
Monish Jain et al.
Journal of medicinal chemistry, 47(15), 3843-3852 (2004-07-09)
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. Kinetic studies demonstrated that all these compounds spontaneously liberate
Reagent effects on distribution of methylsulfonylethyl substituents in the D-glucopyranosyl unit of cotton cellulose.
Rowland SP, et al.
Canadian Journal of Chemistry, 46(3), 451-457 (1968)
Mild conversion of electron deficient aryl fluorides to phenols using 2-(methylsulfonyl) ethanol.
Rogers JF and Green DF.
Tetrahedron Letters, 43(19), 3585-3587 (2002)
Sebastian Bonardd et al.
Polymers, 13(3) (2021-01-28)
In this work, polymethacrylates containing sulfonyl and nitrile functional groups were successfully prepared by conventional radical polymerization and reversible addition-fragmentation chain-transfer polymerization (RAFT). The thermal and dielectric properties were evaluated, for the first time, considering differences in their molecular weights
S G Cohen et al.
Journal of medicinal chemistry, 28(9), 1309-1313 (1985-09-01)
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 binds similarly to its acetate substrate; cationic analogues, (CH3)3N+CH2CH2OH
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