TCI C1309 1,1-Cyclopropanedicarboxylic Acid carries two carboxyl groups on a single carbon of a strained three-membered ring. This gem-disubstituted arrangement makes it a valuable building block for introducing rigid cyclopropane motifs into target molecules. Both acid groups can be converted into esters or amides, or used as handles for ring construction and decarboxylation studies. AMI Scientific offers this TCI product in 1 g and 5 g packs for laboratory research and medicinal chemistry work.
TCI brochures (PDF)
- Biomaterials Research Reagents 2025-02-19 · p. 21
- Monomers 2025-05-28 · p. 34
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- HELL et al. (1996). ChemInform Abstract: Efficient Method for Removal of a Carboxylic Acid Moiety from Sterically Crowded Cyclopropanedicarboxylic Acid Derivatives.. ChemInform doi:10.1002/chin.199636063
- Hell et al. (1996). Efficient Method for Removal of a Carboxylic Acid Moiety from Sterically Crowded Cyclopropanedicarboxylic Acid Derivatives. Synthetic Communications doi:10.1080/00397919608003571
- Kvaratskhelia et al. (2011). The Regularities of Electrolytic Dissociation of 1,2-Cyclopropanedicarboxylic Acids. ECS Transactions doi:10.1149/1.3646092
References were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.







