| Enquire Now |
| Structural formula |
White crystalline solid.
The regio-isomer, 2,3-O-Camphanylidene-D-myo-inositol is also available.
The 1,2- and 2,3-camphanylidene acetals are the key regio-isomeric starting materials to prepare chiral and stereoselective phosphatidyl inositol phosphates and other glycolipids. With these starting materials pure enantiomeric finished forms can be isolated after deprotection (removal of the camphor group).
Formula: C16H26O6
Molecular Weight: 314.37
CAS Number: 128525-54-2
Solubility: Slightly soluble
Pilot scale samples are currently available (POA).
Please refer to K S Bruzik and M-D Tsai, JOC 2003, 68, 960-968 for the synthesis of phosphorylated phosphatidylinositols.
And Manuel Martin-Lomas et al., Chem. Eur. J. 1999, 5, no.1 320-336 for the glycosylation at the 6-OH leading to glycosylphosphatidylinositols (GPI's).
Product known as
1,2-O-Camphanylidene inositol2,3-O-Camphanylidene inositol
1,2-O-(L-1,7,7-trimethyl[2,2,1]bicylohept-6-ylidene)-D-myo-inositol