TCI C0816 2-Cyclohexen-1-ol is a cyclic allylic alcohol combining a hydroxyl group with an adjacent ring double bond. This arrangement gives rise to characteristic allylic reactivity, useful in allylic substitution, directed epoxidation, and Mitsunobu chemistry. It also serves as a direct precursor to cyclohexenone through oxidation and as a common model substrate in catalysis studies. AMI Scientific offers this reagent in a compact package size suited to research and reaction optimisation.
Related TCI products
- TCI T2723 4883-60-7 2-Hydroxy-3,5,5-trimethyl-2-cyclohexen-1-one
- TCI M2455 2699-13-0 3-Methoxycyclohexene
- TCI D5576 21544-03-6 Diglycidyl 4-Cyclohexene-1,2-dicarboxylate
- TCI C2435 1679-51-2 3-Cyclohexene-1-methanol
- TCI A1936 5220-49-5 3-Amino-2-cyclohexen-1-one
- TCI A1300 873-95-0 3-Amino-5,5-dimethyl-2-cyclohexen-1-one
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- Khan et al. (1996). Solvent induced isomerization of 2-cyclohexen-1-ol to 3-cyclohexen-1-ol by a chiral lithium amide. Tetrahedron: Asymmetry doi:10.1016/0957-4166(96)00017-1
- Dezi et al. (1996). Regioselectivity in the Gas‐Phase Nucleophilic Attack on O‐Protonated 3‐Methyl‐2‐cyclohexen‐1‐ol and 1‐Methyl‐2‐cyclohexen‐1‐ol. Chemistry – A European Journal doi:10.1002/chem.19960020314
- BHUNIYA et al. (1994). ChemInform Abstract: Enantioselective Deprotonation of Cyclohexene Oxide to (R)‐2‐ Cyclohexen‐1‐ol.. ChemInform doi:10.1002/chin.199448054
References were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.
Produk Terkait
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