Weight | 100.161 g/mol |
---|---|
Formula | C6H12O |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 1 |
Aromatic Rings | 0 |
Rotatable Bonds | 3 |
trans-2-Hexen-1-Ol (928-95-0, 2305-21-7)
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- Sigma-Aldrich - trans-2-Hexen-1-Ol28.30 - 839.00 USD
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- TCI - trans-2-Hexen-1-Ol40.00 - 202.00 USD
- Rate constants for the gasphase reactions of cis3Hexen1ol, cis3Hexenylacetate, trans2Hexenal, and Linalool with OH and NO3 radicals and O3 at 296 2 K, and OH radical formation yields from the O3 reactions (International Journal of Chemical Kinetics, 1995)
- Phase behavior of the reactants, products and catalysts involved in the allylic epoxidation of trans-2-Hexen-1-ol to (2R,3R)-(+)-3-Propyloxiranemethanol in high pressure carbon dioxide (Journal of Supercritical Fluids, 1998)
- Multicomponent phase equilibrium measurements and modeling for the allylic epoxidation of trans-2-hexen-1-ol to (2R,3R)-(+)-3-propyloxiranemethanol in high-pressure carbon dioxide (Journal of Supercritical Fluids, 2001)
- Physicochemical characterization of vanadium-doped alumina-pillared montmorillonite catalyst: Epoxidation of trans-2-hexen-1-ol (Comptes Rendus Chimie, 2009)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCCC=CCO
-
InChIKeyZCHHRLHTBGRGOT-UHFFFAOYSA-N
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Synthesis
Reactant
+
1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide
(Nicolaou IBX dehydrogenation)
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