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Atomfair (1R,2R)-2-(benzylamino)cyclohexanol C13H19NO

Description (1R,2R)-2-(Benzylamino)cyclohexanol (CAS No. 141553-09-5) is a chiral cyclohexanol derivative with the molecular formula C13H19NO. This compound features a stereospecific (1R,2R) configuration, making it a valuable intermediate in asymmetric synthesis and pharmaceutical research. Its structure includes a benzylamino group and a hydroxyl group on a cyclohexane ring, offering versatile reactivity for derivatization. With a purity grade suitable for research applications, this product is ideal for use in catalysis, ligand design, and medicinal chemistry. Packaged under inert conditions to ensure stability, it is supplied as a solid with detailed analytical data (NMR, HPLC, MS) available upon request.

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Description

Description

(1R,2R)-2-(Benzylamino)cyclohexanol (CAS No. 141553-09-5) is a chiral cyclohexanol derivative with the molecular formula C13H19NO. This compound features a stereospecific (1R,2R) configuration, making it a valuable intermediate in asymmetric synthesis and pharmaceutical research. Its structure includes a benzylamino group and a hydroxyl group on a cyclohexane ring, offering versatile reactivity for derivatization. With a purity grade suitable for research applications, this product is ideal for use in catalysis, ligand design, and medicinal chemistry. Packaged under inert conditions to ensure stability, it is supplied as a solid with detailed analytical data (NMR, HPLC, MS) available upon request.

  • CAS No: 141553-09-5
  • Molecular Formula: C13H19NO
  • Molecular Weight: 205.30
  • Exact Mass: 205.146664230
  • Monoisotopic Mass: 205.146664230
  • IUPAC Name: (1R,2R)-2-(benzylamino)cyclohexan-1-ol
  • SMILES: C1CC[C@H]([C@@H](C1)NCC2=CC=CC=C2)O
  • Synonyms: (1R,2R)-2-(benzylamino)cyclohexanol, 40571-86-6, 141553-09-5, trans-2-(Benzylamino)cyclohexanol, (1R,2R)-2-(benzylamino)cyclohexan-1-ol

Application

(1R,2R)-2-(Benzylamino)cyclohexanol is widely utilized as a chiral building block in the synthesis of pharmaceuticals and agrochemicals. Its stereochemistry makes it a key precursor for asymmetric hydrogenation and other enantioselective transformations. Researchers employ this compound in the development of ligands for transition-metal catalysis. It also serves as a scaffold for studying biological activity in CNS-targeting molecules. Additionally, it finds use in academic and industrial settings for method development in organic synthesis.

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