TCI C1463 cis-1,2-Cyclohexanediamine is an alicyclic diamine bearing two adjacent primary amine groups in the cis configuration. It serves as a versatile bidentate ligand for transition metal complexes and as a precursor to Schiff bases, ureas, amides, and macrocyclic frameworks. The rigid cyclohexane backbone provides well-defined conformational control that is valuable in coordination chemistry and catalysis research. AMI Scientific offers this reagent in original TCI packaging, and users should handle it under dry conditions because primary amines readily react with atmospheric moisture and carbon dioxide.
Related TCI products
- TCI D4740 885280-64-8 N,N-Dimethyl-1,3-cyclohexanediamine (cis- and trans- mixture)
- TCI D4566 42389-54-8 N,N-Diethyl-1,4-cyclohexanediamine (cis- and trans- mixture)
- TCI D4288 42389-50-4 N,N-Dimethyl-1,4-cyclohexanediamine (cis- and trans- mixture)
- TCI D0277 694-83-7 1,2-Cyclohexanediamine (cis- and trans- mixture)
- TCI C1426 2615-25-0 trans-1,4-Cyclohexanediamine
- TCI C1120 1121-22-8 trans-1,2-Cyclohexanediamine
—
| Brand | — |
|---|---|
| CAS number | — |
| Molecular formula | — |
| Purity | — |
| Category | — |
| Pack sizes | — |
| Physical form | — |
| Storage | — |
—
- Lee et al. (2018). Practical synthesis of four different pseudoenantiomeric organocatalysts with both cis- and trans-substituted 1,2-cis-cyclohexanediamine structures from a common intermediate. Tetrahedron doi:10.1016/j.tet.2018.05.035
- Lee et al. (2017). Practical Synthesis of Two Different Pseudoenantiomeric Organocatalysts with cis‐Cyclohexanediamine Structure from a Common Chiral Source. Asian Journal of Organic Chemistry doi:10.1002/ajoc.201700229
References were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.





