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.
Related TCI products
- TCI M2492 4342-60-3 4-Methyl-3-cyclohexene-1-carboxylic Acid
- TCI C0652 4771-80-6 3-Cyclohexene-1-carboxylic Acid
- TCI T2723 4883-60-7 2-Hydroxy-3,5,5-trimethyl-2-cyclohexen-1-one
- TCI A1936 5220-49-5 3-Amino-2-cyclohexen-1-one
- TCI T0605 2915-49-3 Bis(2-ethylhexyl) 4-Cyclohexene-1,2-dicarboxylate
- TCI M1190 5333-84-6 3-Methyl-4-cyclohexene-1,2-dicarboxylic Anhydride
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- 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.
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4-Methyl-3-cyclohexene-1-carboxylicAcid TCI M2492
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