| Weight | 195.24 g/mol |
|---|---|
| Formula | C6H13NO4S |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 3 |
4432-31-9 (4432-31-9)
MES compound · 4-morpholineethanesulfonate · 2-(N-morpholino)ethanesulfonic acid
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- [2,6-Mes2C6H3]2Ga+Li[Al{OCH(CF3)2}4]2- (Mes = 2,4,6-Me3C6H2): A compound containing a linear unsolvated two-coordinate gallium cation (Journal of the American Chemical Society, 2003)
- Induction of polymerization of purified tubulin by sulfonate buffers. Marked differences between 4-morpholineethanesulfonate (Mes) and 1,4-piperazineethanesulfonate (Pipes). (FEBS Journal, 1981)
- First characterization of a compound with a tingermanium double bond: the dimesityl(diisitylstanna)germene (Is)2SnGe(Mes)2 (Chemical Communications, 1996)
- Method of making MES field effect transistor using III-V compound semiconductor (1992)
- Molecular SelfAssembly to Give the Antiferromagnetic Cage Compound [{CpFe(CO)2(Mes)PO2}4{MesPO3Fe2(OH)Cl}2] (Angewandte Chemie, 1997)
- The synthetic compound 2-hydroxy-2,4,6-trimethoxychalcone overcomes P-glycoprotein-mediated multi-drug resistance in drug-resistant uterine sarcoma MES-SA/DX5 cells (Journal of The Korean Society for Applied Biological Chemistry, 2015)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - MES compound
- 4-morpholineethanesulfonate
- 2-(N-morpholino)ethanesulfonic acid
- 2-morpholinoethanesulfonate
- 2-(N-morpholino)ethanesulfonic acid, sodium salt
-
SMILESC1COCCN1CCS(=O)(=O)O
-
InChIKeySXGZJKUKBWWHRA-UHFFFAOYSA-N
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