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About This Item
線性公式:
CH3SO2CH2CH2OH
CAS號碼:
分子量：:
124.16
Beilstein:
1746915
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
推薦產品
化驗
98%
bp
148-149 °C (lit.)
mp
31-33 °C (lit.)
SMILES 字串
CS(=O)(=O)CCO
InChI
1S/C3H8O3S/c1-7(5,6)3-2-4/h4H,2-3H2,1H3
InChI 密鑰
KFTYFTKODBWKOU-UHFFFAOYSA-N
尋找類似的產品？ 前往 產品比較指南
一般說明
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.
應用
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.
訊號詞
Warning
危險聲明
危險分類
Skin Sens. 1
儲存類別代碼
10 - Combustible liquids
水污染物質分類（WGK）
WGK 3
閃點（°F）
235.4 °F - closed cup
閃點（°C）
113.00 °C - closed cup
個人防護裝備
Eyeshields, Gloves
分析證明 (COA)
輸入產品批次/批號來搜索 分析證明 (COA)。在產品’s標籤上找到批次和批號，寫有 ‘Lot’或‘Batch’.。
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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