Product Name: (1S,2S,3R,5S)-(+)-2,3-Pinanediol
Synonyms: (+)-2-Hydroxyisopinocampheol,( 57364469, 57186162,1S,2S,3R,5S)-2,3-Pinanediol,( 57364470, 57186163,1S,2S,3R,5S)-2,6,6-Trimethylbicyclo[3.1.1]heptane-2,3-diol, [1S-(1α,2α,3α,5α)]-2,6,6-Trimethylbicyclo[3.1.1]heptane-2,3-diol;(+)-2-Hydroxyisopinocampheol,( 57364471, 57186164,1S,2S,3R,5S)-2,6,6-Trimethylbicyclo[3.1.1]heptane-2,3-diol;[1S-(1α,2α,3α,5α)]-2,6,6-Trimethylbicyclo[3.1.1]heptane-2,3-diol;(1S, 2S, 3R, 5S)-(+)Pinanediol (Bortezomib Intermediate);(1S,2S,3R,5S)-(+)-2;(+)-pinanendiol;cis-2,3-Pinandiol;(1S,2S,3R,5S)-(+)-Pinanediol,( 57364472, 57186165,1S,2S,3R,5S)-(+)-2,3-Dihydroxy-2,6,6-trimethylbicyclo[3.1.1]heptane
CAS: 18680-27-8
MF: C10H18O2
MW: 170.25
EINECS: 606-096-6
Product Categories: Chiral Compounds
Melting point 57-59 °C(lit.)
alpha 8.5 º (c=6.5, toluene)
Boiling point 239.9°C (rough estimate)
density 0.9409 (rough estimate)
refractive index 1.4494 (estimate)
Fp >230 °F
storage temp. 2-8°C
form Crystalline Powder, Crystals or Mass
color White to light beige
Uses (1S,2S,3R,5S)-(+)-2,3-Pinanediol is a bicyclic monoterpene diols that has been shown to induce differentiation of S91 melanoma and PC12 pheochromocytoma cells and thus provide possible therapeutic and sunless tanning use. It is also used in the transformation of isopinocampheol and caryophyllene oxide.