(R)-2-amino-2-(naphthalen-2-yl)ethanol

95%

Reagent Code: #230879
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CAS Number 204851-80-9

science Other reagents with same CAS 204851-80-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 187.24 g/mol
Formula C₁₂H₁₃NO
badge Registry Numbers
MDL Number MFCD09253743
thermostat Physical Properties
Boiling Point 392.9±22.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.182±0.06 g/cm3(Predicted)
Storage 2-8°C, light-proof storage, inert atmosphere

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of β-adrenergic receptor blockers and other bioactive molecules. Its rigid naphthyl group and chiral amino alcohol structure make it valuable in asymmetric synthesis and catalysis. Also employed in the preparation of ligands for enantioselective transformations. Shows potential in medicinal chemistry for designing enzyme inhibitors due to its structural similarity to natural amino alcohols.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿18,920.00
250mg
10-20 days ฿28,370.00
1g
10-20 days ฿87,040.00
(R)-2-amino-2-(naphthalen-2-yl)ethanol
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of β-adrenergic receptor blockers and other bioactive molecules. Its rigid naphthyl group and chiral amino alcohol structure make it valuable in asymmetric synthesis and catalysis. Also employed in the preparation of ligands for enantioselective transformations. Shows potential in medicinal chemistry for designing enzyme inhibitors due to its structural similarity to natural amino alcohols.

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of β-adrenergic receptor blockers and other bioactive molecules. Its rigid naphthyl group and chiral amino alcohol structure make it valuable in asymmetric synthesis and catalysis. Also employed in the preparation of ligands for enantioselective transformations. Shows potential in medicinal chemistry for designing enzyme inhibitors due to its structural similarity to natural amino alcohols.

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