TCI C1448 (1S,2S)-(+)-1,2-Cyclohexanediamine (CAS 21436-03-3) is the enantiomeric counterpart of the widely used trans-1,2-diaminocyclohexane scaffold. It allows researchers to reverse the sense of chiral induction while keeping the same catalytic system, giving access to either product enantiomer. Typical uses include salen and Schiff base ligand synthesis, transition metal complexation, and hydrogen-bonding organocatalysts. AMI Scientific offers this TCI product in 5 g and 25 g packs, to be handled under the manufacturer's recommended inert and dry conditions.
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Related TCI products
- TCI C1447 20439-47-8 (1R,2R)-(-)-1,2-Cyclohexanediamine
- TCI B3483 365996-30-1 (1S,2R)-N1-(tert-Butoxycarbonyl)-1,2-cyclohexanediamine
- TCI B3478 364385-54-6 (1R,2S)-N1-(tert-Butoxycarbonyl)-1,2-cyclohexanediamine
- TCI C1450 67333-70-4 (1S,2S)-(-)-1,2-Cyclohexanediamine D-Tartrate
- TCI C1449 39961-95-0 (1R,2R)-(+)-1,2-Cyclohexanediamine L-Tartrate
- TCI B5648 180683-64-1 (1S,2S)-N1-(tert-Butoxycarbonyl)-1,2-cyclohexanediamine
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- Garbutcheon-Singh et al. (2016). Synthesis, characterisation and cytotoxicity of [(1,10-phenanthroline)(1R,2R,4R/1S,2S,4S)-4-methyl-1,2-cyclohexanediamine)platinum(II)]2+ (PHEN-4-MeDACH). Inorganica Chimica Acta doi:10.1016/j.ica.2015.10.048
- Zhang et al. (2010). Fixed helical Cd(II) coordination polymers assembled from diastereopure Schiff-base ligands derived from condensation of acetylacetone with 1S,2S- and 1R,2R-cyclohexanediamine. Inorganic Chemistry Communications doi:10.1016/j.inoche.2010.05.015
- Kaizaki et al. (1998). First solid state synthesis of the racemic compound and enantiomer of dinuclear Λ,Λ-di-μ-hydroxo-bis [bis((1S,2S)-1,2-transcyclohexanediamine)chromium(III)] and Δ,Δ-di-μ-hydroxo-bis [bis((1R, 2R)-1,2-trans-cyclohexanediamine) chromium (III)] bromides. Inorganica Chimica Acta doi:10.1016/s0020-1693(97)06093-3
References were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.





