Pinpollitol

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Pinpollitol
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Names
IUPAC name
1D-1,4-Di-O-methyl-chiro-inositol
Systematic IUPAC name
(1R,2R,3R,4S,5R,6S)-3,6-Dimethoxycyclohexane-1,2,4,5-tetrol
Other names
1,4-Di-O-Methyl-D-chiro-inositol
Identifiers
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3D model (JSmol)
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  • InChI=1S/C8H16O6/c1-13-7-3(9)5(11)8(14-2)6(12)4(7)10/h3-12H,1-2H3/t3-,4-,5-,6+,7-,8+/m1/s1 checkY
    Key: DYQWYDODKPTUPA-CUYQCCFGSA-N checkY
  • InChI=1/C8H16O6/c1-13-7-3(9)5(11)8(14-2)6(12)4(7)10/h3-12H,1-2H3/t3-,4-,5-,6+,7-,8+/m1/s1
  • CO[C@@H]1[C@@H]([C@H]([C@@H]([C@H]([C@H]1O)O)OC)O)O
Properties
C8H16O6
Molar mass 208.210 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

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Pinpollitol is a cyclitol. It is a di-O-methyl-(+)-chiro-inositol that can be isolated from Pinus radiata.[1]

References

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  1. ^ Page Module:Citation/CS1/styles.css has no content.Gallagher, R (1975). "(+)-Pinpollitol: A di-O-methyl D-(+)-chiro-inositol from Pinus radiata". Phytochemistry. 14 (3): 755–757. Bibcode:1975PChem..14..755G. doi:10.1016/0031-9422(75)83029-9.


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