Pinpollitol

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Pinpollitol

IUPAC name (1R,2R,3R,4S,5R,6S)-3,6-Dimethoxycyclohexane-1,2,4,5-tetraol
Other names 1,4-Di-O-Methyl-D-chiro-inositol
Identifiers
CAS number	56246-31-2^Y
ChemSpider	24764944^Y
Jmol-3D images	{{#if:CO[C@@H]1[C@@H]([C@H]([C@@H]([C@H]([C@H]1O)O)OC)O)O\|Image 1
SMILES CO[C@@H]1[C@@H]([C@H]([C@@H]([C@H]([C@H]1O)O)OC)O)O
InChI 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^Y Key: DYQWYDODKPTUPA-CUYQCCFGSA-N^Y 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
Properties
Molecular formula	C₈H₁₆O₆
Molar mass	208.21 g mol⁻¹
Y (verify) (what is: Y/N?) Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
Infobox references

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

References

↑ Gallagher, R (1975). "(+)-Pinpollitol: A di-O-methyl D-(+)-chiro-inositol from Pinus radiata". Phytochemistry 14: 755. doi:10.1016/0031-9422(75)83029-9.

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