Chemistry:2-Methylthioethylamine
From HandWiki
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| Names | |
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| Preferred IUPAC name
2-(Methylsulfanyl)ethan-1-amine | |
| Other names
2-(Methylthio)ethylamine; 2-Aminoethyl methyl sulfide; S-Methylcysteamine
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| Identifiers | |
3D model (JSmol)
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PubChem CID
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CompTox Dashboard (EPA)
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| Properties | |
| C3H9NS | |
| Molar mass | 91.17 g·mol−1 |
| Appearance | Colorless liquid |
| Boiling point | 146–148 °C (295–298 °F; 419–421 K) |
| Hazards | |
| GHS pictograms |  
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| GHS Signal word | Danger |
| H226, H314 | |
| P210, P233, P240, P241, P242, P243, P260, P264, P280, P301+330+331, P303+361+353, P304+340, P305+351+338, P310, P321, P363, P370+378, P403+235, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
2-Methylthioethylamine is the organosulfur compound with the formula CH3SCH2CH2NH2. It is a colorless liquid. It can be viewed as the product of S-methylation of cysteamine or decarboxylation of S-methylcysteine. The compound is a ligand and, via Schiff base condensations, a ligand precursor.[1]
References
- ↑ Tshuva, Edit Y.; Groysman, Stanislav; Goldberg, Israel; Kol, Moshe; Goldschmidt, Zeev (2002). "[ONXO]-Type Amine Bis(phenolate) Zirconium and Hafnium Complexes as Extremely Active 1-Hexene Polymerization Catalysts". Organometallics 21 (4): 662–670. doi:10.1021/om010493w.
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