2-Methylserine
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| Names | |
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| IUPAC name
α-methyl-serine
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| Systematic IUPAC name
2-Amino-3-hydroxy-2-methylpropanoic acid | |
| Identifiers | |
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3D model (JSmol)
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| ChEBI |
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| ChEMBL |
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| ChemSpider |
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| ECHA InfoCard | 100.024.150 |
| KEGG |
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| MeSH | 2-methylserine |
PubChem CID
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CompTox Dashboard (EPA)
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| Properties | |
| C4H9NO3 | |
| Molar mass | 119.120 g·mol−1 |
| soluble | |
| Hazards | |
| GHS labelling: | |
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| Warning | |
| H315, H319, H335 | |
| P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
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2-Methylserine is a non-proteinogenic amino acid that is structurally similar to serine. Like serine, it is polar, and therefore soluble in water. It differs structurally from serine by the presence of a methyl group on the backbone carbon.
2-Methylserine is one of the amino acids produced by an unpublished volcanic-spark discharge experiment conducted by Stanley Miller in the early 1950s. However, the presence of this and many other organic compounds was not discovered until Jeffrey Bada et al. re-analyzed the contents of the vials from Miller's experiment in 2008.[1]
References
- ^ Johnson, Adam P.; Cleaves, H. James; Dworkin, Jason P.; Glavin, Daniel P.; Lazcano, Antonio; Bada, Jeffrey L. (2008-10-17). "The Miller Volcanic Spark Discharge Experiment". Science. 322 (5900): 404. Bibcode:2008Sci...322..404J. doi:10.1126/science.1161527. ISSN 0036-8075. PMID 18927386.
Further reading
- Anson, Michael S.; Clark, Hugh F.; Evans, Paul; Fox, Martin E.; Graham, Jonathan P.; Griffiths, Natalie N.; Meek, Graham; Ramsden, James A.; Roberts, Alastair J.; Simmonds, Shaun; Walker, Matthew D.; Willets, Matthew (2011-03-18). "Complementary Syntheses of N,O-Protected-(S)-2-methylserine on a Multikilogram Scale". Organic Process Research & Development. 15 (2): 389–397. doi:10.1021/op100299d. ISSN 1083-6160.

