| Revision as of 17:42, 19 August 2011 editCheMoBot (talk | contribs)Bots141,565 edits Updating {{chembox}} (no changed fields - added verified revid - updated 'DrugBank_Ref', 'UNII_Ref', 'ChEMBL_Ref', 'ChEBI_Ref', 'KEGG_Ref', 'ChEBI_Ref') per Chem/Drugbox validation (report [[Wiki← Previous edit | Revision as of 05:36, 20 March 2012 edit undoRezabot (talk | contribs)Extended confirmed users48,194 editsm r2.7.1) (Robot: Adding fa:متاناتیولات سدیمNext edit → | ||
| Line 38: | Line 38: | ||
| {{organic-compound-stub}} | {{organic-compound-stub}} | ||
| ] | |||
Revision as of 05:36, 20 March 2012
For sodium 2-mercaptoethanesulfonate, see Mesna.
| |
| Names | |
|---|---|
| IUPAC name sodium methanethiolate | |
| Other names sodium thiomethoxide, sodium methyl mercaptide, sodium thiomethylate, methanethiol sodium salt, methyl mercaptan sodium salt | |
| Identifiers | |
| CAS Number | |
| 3D model (JSmol) | |
| ChemSpider | |
| ECHA InfoCard | 100.023.609 
|
| EC Number |
|
| PubChem CID | |
| CompTox Dashboard (EPA) | |
InChI
| |
SMILES
| |
| Properties | |
| Chemical formula | CH3NaS |
| Molar mass | 70.08 g·mol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa).
 Y verify (what is ?)
Infobox references
| |
Sodium methanethiolate or sodium thiomethoxide (CH3SNa, MeSNa) is the sodium conjugate base of methanethiol. This compound is commercially available as a white solid. It is a powerful nucleophile that can be used to prepare methylthioethers. Its hydrolysis in moist air produces methanethiol, which has a low odor threshold and a noxious fecal smell.
 | This article about an organic compound is a stub. You can help Misplaced Pages by expanding it. |