TCI C1296 1-Cyclohexene-1-carboxylic Acid is an α,β-unsaturated cyclic carboxylic acid offering two complementary reactive sites. The carboxyl group supports amide, ester, and acid chloride formation, while the conjugated alkene enables epoxidation, dihydroxylation, and catalytic hydrogenation. It is frequently chosen as a model substrate when evaluating chiral catalysts in asymmetric hydrogenation studies. AMI Scientific offers this TCI building block in 1 g and 5 g pack sizes for small to medium scale research.
—
| Brand | — |
|---|---|
| CAS number | — |
| Molecular formula | — |
| Purity | — |
| Category | — |
| Pack sizes | — |
| Physical form | — |
| Storage | — |
—
- Wang et al. (2014). Dehydro-aromatization of cyclohexene-carboxylic acids by sulfuric acid: critical route for bio-based terephthalic acid synthesis. RSC Advances doi:10.1039/c3ra46670a
- Geiger et al. (1995). (3S,4S,5R)-3,4,5-trihydroxy-1-cyclohexene-carboxylic acid from Sequoiadendron giganteum. Phytochemistry doi:10.1016/0031-9422(95)00450-l
- Xu et al. (2020). Facile access to chiral β-homoglutamic acid from 3-cyclohexene-carboxylic acid. Synthetic Communications doi:10.1080/00397911.2020.1802760
References were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.
