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TCI

CAS 17430-98-7

(S)-(+)-1-Cyclohexylethylamine TCI C1531

(S)-(+)-1-Cyclohexylethylamine TCI C1531

Chemical Identity

Other names
(S)-(+)-(1-Aminoethyl)cyclohexane
CAS No.
17430-98-7
PubChem
CID 5325951·SID 87566528
Formula
C8H17N
Molecular weight
127.23 g/mol
Purity
>98.0%(GC)(T)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
(1S)-1-cyclohexylethanamine
SMILES
CC(C1CCCCC1)N
InChIKey
XBWOPGDJMAJJDG-ZETCQYMHSA-N
MDL
MDL00066261
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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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  • 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.