Pinpollitol

Pinpollitol
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
CAS Number	56246-31-2 ;
3D model (JSmol)	Interactive image;
ChemSpider	24764944 ;
PubChem CID	7099087;
CompTox Dashboard (EPA)	DTXSID10427769 ;
	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 Key: DYQWYDODKPTUPA-CUYQCCFGSA-N ; 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;
	SMILES CO[C@@H]1[C@@H]([C@H]([C@@H]([C@H]([C@H]1O)O)OC)O)O;
Properties
Chemical formula	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). verify (what is ?) 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 (3): 755–757. doi:10.1016/0031-9422(75)83029-9.

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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
CAS Number	56246-31-2^Y
3D model (JSmol)	Interactive image
ChemSpider	24764944^Y
PubChem CID	7099087
CompTox Dashboard (EPA)	DTXSID10427769
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
SMILES CO[C@@H]1[C@@H]([C@H]([C@@H]([C@H]([C@H]1O)O)OC)O)O
Properties
Chemical formula	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). Y verify (what is ^YN ?) Infobox references