(1S,2S)-()-1-Amino-2-indanol

98%

Reagent Code: #235303
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CAS Number 163061-74-3

science Other reagents with same CAS 163061-74-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 149.19 g/mol
Formula C₉H₁₁NO
badge Registry Numbers
MDL Number MFCD08275383
thermostat Physical Properties
Melting Point 146°C
inventory_2 Storage & Handling
Storage Room temperature, stored in inert gas

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of protease inhibitors like Crixivan (indinavir), which is used to treat HIV. Its rigid indane structure and well-defined stereochemistry make it ideal for controlling stereoselectivity in drug synthesis. Also employed in asymmetric synthesis and as a ligand or intermediate in catalytic reactions. Its ability to form stable intermediates enhances efficiency in multi-step organic transformations.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿660.00
inventory 1g
10-20 days ฿2,520.00
inventory 5g
10-20 days ฿11,700.00
(1S,2S)-()-1-Amino-2-indanol
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of protease inhibitors like Crixivan (indinavir), which is used to treat HIV. Its rigid indane structure and well-defined stereochemistry make it ideal for controlling stereoselectivity in drug synthesis. Also employed in asymmetric synthesis and as a ligand or intermediate in catalytic reactions. Its ability to form stable intermediates enhances efficiency in multi-step organic transformations.

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of protease inhibitors like Crixivan (indinavir), which is used to treat HIV. Its rigid indane structure and well-defined stereochemistry make it ideal for controlling stereoselectivity in drug synthesis. Also employed in asymmetric synthesis and as a ligand or intermediate in catalytic reactions. Its ability to form stable intermediates enhances efficiency in multi-step organic transformations.

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