TCI (S)-(+)-1-Cyclohexylethylamine (CAS 17430-98-7) is an enantiomerically defined chiral primary amine bearing a bulky cyclohexyl group. It is commonly used as a resolving agent for racemic carboxylic acids via diastereomeric salt formation, and as a removable chiral auxiliary in asymmetric synthesis. The compound also serves as a starting material for chiral ligands and as a derivatising reagent in enantiomeric purity analysis. AMI Scientific supplies 5 g and 25 g packs; keep tightly sealed away from air and moisture, and consult the manufacturer's Safety Data Sheet and Certificate of Analysis.
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Related TCI products
- TCI C1541 5913-13-3 (R)-(-)-1-Cyclohexylethylamine
- TCI C2765 4442-85-7 2-Cyclohexylethylamine
- TCI T3614 75-50-3 Trimethylamine (ca. 8% in Toluene, ca. 1mol/L)
- TCI T2893 75-50-3 Trimethylamine (ca. 25% in Isopropyl Alcohol, ca. 3mol/L)
- TCI T1181 75-22-9 Trimethylamine Borane
- TCI A1494 6270-07-1 N-Acetyl-2-(4-nitrophenyl)ethylamine
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- Sakai et al. (2006). Molecular mechanism of DCR phenomenon observed in (RS)-1-cyclohexylethylamine–mandelic acid resolution system. Tetrahedron: Asymmetry doi:10.1016/j.tetasy.2006.06.037
- Patel et al. (2012). Functionalization of Keggin type manganese substituted phosphotungstate by R-(−)-1-cyclohexylethylamine: Synthesis and characterization. Inorganica Chimica Acta doi:10.1016/j.ica.2011.10.017
- Turani‐I‐Belloto et al. (2023). Synthesis and Characterization of (R)‐N‐1‐Cyclohexylethylamine Borane. ChemistrySelect doi:10.1002/slct.202301646
References were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.

