Chemistry:Neo-Inositol
From HandWiki
| |
| Names | |
|---|---|
| IUPAC name
neo-Inositol[1]
| |
| Systematic IUPAC name
(1R,2R,3s,4S,5S,6s)-Cyclohexane-1,2,3,4,5,6-hexol | |
| Identifiers | |
3D model (JSmol)
|
|
| ChEBI | |
| ChemSpider | |
| UNII | |
| |
| |
| Properties | |
| C6H12O6 | |
| Molar mass | 180.156 g·mol−1 |
| Melting point | 315 °C; 599 °F; 588 K[2] |
| Hazards | |
| Main hazards | Irritating to eyes, respiratory system and skin.[3] |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
 verify (what is   ?)
| |
| Infobox references | |
neo-Inositol is one of the stereoisomers of inositol. It is one of the nine isomeric forms of cyclohexanehexol; a group of small and chemically very stable polar molecules that have versatile properties.[4] This stereoisomer is naturally occurring, but only in small amounts. It is also known as (1s,2R,3R,4s,5S,6S)-cyclohexane-1,2,3,4,5,6-hexol or 1,2,3/4,5,6-cyclohexanehexol in the IUPAC naming system.[5]
See also
- allo-Inositol
- cis-Inositol
- D-chiro-Inositol
- L-chiro-Inositol
- epi-Inositol
- muco-Inositol
- scyllo-Inositol
References
- ↑ International Union of Pure and Applied Chemistry (2014). Nomenclature of Organic Chemistry: IUPAC Recommendations and Preferred Names 2013. The Royal Society of Chemistry. pp. 1415. doi:10.1039/9781849733069. ISBN 978-0-85404-182-4.
- ↑ Watt, S. W.; Chisholm, J. A.; Jones, W.; Motherwell, S. (2004). "A Molecular Dynamics Simulation of the Melting Points and Glass Transition Temperatures of Myo- and Neo-Inositol". Journal of Chemical Physics 121 (19): 9565–9573. doi:10.1063/1.1806792. PMID 15538878.
- ↑ "Material Safety Data Sheet". Sigma-Aldrich. http://www.sigmaaldrich.com/MSDS/MSDS/DisplayMSDSPage.do?country=US&language=en&productNumber=516163&brand=ALDRICH&PageToGoToURL=http%3A%2F%2Fwww.sigmaaldrich.com%2Fcatalog%2Fproduct%2Faldrich%2F516163%3Flang%3Den. Retrieved 9 October 2012.
- ↑ Michell, R. H. (February 2008). "Inositol Derivatives: Evolution and Functions". Nature Reviews Molecular Cell Biology 9 (2): 151–61. doi:10.1038/nrm2334. PMID 18216771. http://xa.yimg.com/kq/groups/15186538/1872049761/name/panthini.pdf.
- ↑ "Neo-Inositol". http://www.ebi.ac.uk/chebi/searchId.do;jsessionid=B128111F38B12846027AAFB90CCC28A6?chebiId=25492. Retrieved 9 October 2012.
 |  |
