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线性分子式:
NH2CONHSO2OCH2CCl3
化学文摘社编号:
分子量:
271.51
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352101
MDL number:
Assay:
96%
Form:
solid
InChI
1S/C3H5Cl3N2O4S/c4-3(5,6)1-12-13(10,11)8-2(7)9/h1H2,(H3,7,8,9)
SMILES string
NC(=O)NS(=O)(=O)OCC(Cl)(Cl)Cl
InChI key
QYUJBOJJEGIBCJ-UHFFFAOYSA-N
assay
96%
form
solid
mp
161-165 °C
Application
用于环脲的合成。
用于铑催化的脲合成。
- Reactant for oxidative C-H amination reactions
Mihyong Kim et al.
Organic letters, 8(6), 1073-1076 (2006-03-10)
[reaction: see text] Oxidative C-H amination of N-trichloroethoxysulfonyl-protected ureas and guanidines is demonstrated to proceed in high yield for tertiary and benzylic-derived substrates. The success of these reactions is predicated on the choice of the electron-withdrawn 2,2,2-trichloroethoxysulfonyl (Tces) protecting group
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