((1R,2R)-2-AMINO-CYCLOHEXYL)-METHANOL

≥95%

Reagent Code: #229089
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CAS Number 5691-15-6

science Other reagents with same CAS 5691-15-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 129.2 g/mol
Formula C₇H₁₅NO
badge Registry Numbers
MDL Number MFCD09834085
thermostat Physical Properties
Boiling Point 82-85 °C
inventory_2 Storage & Handling
Density 0.974±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of enzyme inhibitors and receptor agonists. Its rigid cyclohexyl backbone and two functional groups (amino and hydroxyl) make it valuable for designing compounds with high selectivity and binding affinity. Commonly employed in medicinal chemistry for optimizing pharmacokinetic properties such as solubility and metabolic stability. Also utilized in asymmetric synthesis and as a ligand precursor in catalysis.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿29,700.00
500mg
10-20 days ฿59,390.00
((1R,2R)-2-AMINO-CYCLOHEXYL)-METHANOL
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of enzyme inhibitors and receptor agonists. Its rigid cyclohexyl backbone and two functional groups (amino and hydroxyl) make it valuable for designing compounds with high selectivity and binding affinity. Commonly employed in medicinal chemistry for optimizing pharmacokinetic properties such as solubility and metabolic stability. Also utilized in asymmetric synthesis and as a ligand precursor in catalysi

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of enzyme inhibitors and receptor agonists. Its rigid cyclohexyl backbone and two functional groups (amino and hydroxyl) make it valuable for designing compounds with high selectivity and binding affinity. Commonly employed in medicinal chemistry for optimizing pharmacokinetic properties such as solubility and metabolic stability. Also utilized in asymmetric synthesis and as a ligand precursor in catalysis.

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