2,2,2-Trichloroethoxysulfonamide - CAS 69226-51-3
Catalog: |
BB033741 |
Product Name: |
2,2,2-Trichloroethoxysulfonamide |
CAS: |
69226-51-3 |
Synonyms: |
2,2,2-trichloroethyl sulfamate |
IUPAC Name: | 2,2,2-trichloroethyl sulfamate |
Description: | 2,2,2-Trichloroethoxysulfonamide (CAS# 69226-51-3 ) is a useful research chemical. |
Molecular Weight: | 228.48 |
Molecular Formula: | C2H4Cl3NO3S |
Canonical SMILES: | C(C(Cl)(Cl)Cl)OS(=O)(=O)N |
InChI: | InChI=1S/C2H4Cl3NO3S/c3-2(4,5)1-9-10(6,7)8/h1H2,(H2,6,7,8) |
InChI Key: | VOKONKGVTXWZJI-UHFFFAOYSA-N |
Boiling Point: | 288.7 °C at 760 mmHg |
Density: | 1.801 g/cm3 |
Appearance: | White to yellow powder |
MDL: | MFCD01683146 |
LogP: | 2.35780 |
Publication Number | Title | Priority Date |
KR-20210084996-A | Semiconductor material and manufacturing method thereof | 20191230 |
WO-2021130255-A1 | Dihydro-cyclopenta-isoquinoline derivatives | 20191223 |
CN-110776442-A | Preparation method of memantine hydrochloride intermediate | 20191016 |
CN-108440344-A | A kind of fatty amine preparation method that efficient mechanical force promotes | 20180428 |
CN-108440344-B | Preparation method of fatty amine promoted by mechanical force | 20180428 |
PMID | Publication Date | Title | Journal |
11965370 | 20020506 | The mechanism of the irreversible inhibition of estrone sulfatase (ES) through the consideration of a range of methane- and amino-sulfonate-based compounds | Bioorganic & medicinal chemistry letters |
Complexity: | 189 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 226.897747 |
Formal Charge: | 0 |
Heavy Atom Count: | 10 |
Hydrogen Bond Acceptor Count: | 4 |
Hydrogen Bond Donor Count: | 1 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 226.897747 |
Rotatable Bond Count: | 2 |
Topological Polar Surface Area: | 77.8 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 0.8 |
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