Atomfair (1R,2R)-2-(Cyclopropylamino)cyclohexan-1-ol C9H17NO CAS 189362-43-4

Description

(1R,2R)-2-(Cyclopropylamino)cyclohexan-1-ol (CAS No. 189362-43-4) is a chiral cyclohexanol derivative with a molecular formula of C₉H₁₇NO. This high-purity compound is specifically designed for researchers and scientists working in pharmaceutical development, asymmetric synthesis, and medicinal chemistry. Its stereospecific (1R,2R) configuration makes it a valuable intermediate for the synthesis of enantiomerically pure compounds, particularly in the study of bioactive molecules and receptor interactions. The cyclopropylamino group introduces unique steric and electronic properties, enhancing its utility in structure-activity relationship (SAR) studies. Available in research quantities, this product is rigorously characterized by HPLC, NMR, and mass spectrometry to ensure >98% chemical and enantiomeric purity, meeting the stringent demands of academic and industrial laboratories.

Properties

• CAS Number: 189362-43-4
• Complexity: 134
• IUPAC Name: (1R,2R)-2-(cyclopropylamino)cyclohexanol
• InChI: InChI=1S/C9H17NO/c11-9-4-2-1-3-8(9)10-7-5-6-7/h7-11H,1-6H2/t8-,9-/m1/s1
• InChI Key: CFEAMNVUJMQGNK-RKDXNWHRSA-N
• Exact Mass: 155.131014166
• Molecular Formula: C9H17NO
• Molecular Weight: 155.24
• SMILES: C1CC[C@H]([C@@H](C1)NC2CC2)O
• Topological: 32.3
• Monoisotopic Mass: 155.131014166
• Synonyms: 189362-43-4, (1R,2R)-2-(Cyclopropylamino)cyclohexan-1-ol, DTXSID70573155, DTXCID60523927, (1R,2R)-2-(Cyclopropylamino)cyclohexanol, (1R,2R)-2-CYCLOPROPYLAMINO CYCLOHEXANOL, SCHEMBL7803984, CFEAMNVUJMQGNK-RKDXNWHRSA-N, AKOS006309847, DB-189584, EN300-1234887, trans-N-(2-hydroxycyclohexyl)-N-cyclopropylamine

This compound serves as a key chiral building block in the synthesis of pharmacologically active molecules, particularly those targeting central nervous system (CNS) receptors. Its rigid cyclohexanol scaffold with a cyclopropylamino substituent is useful for probing steric constraints in enzyme inhibition studies. Researchers also employ it as a ligand precursor in asymmetric catalysis and as a template for developing novel antidepressants or neuroprotective agents.

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