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

98%

Reagent Code: #234218
label
Alias (1S,2R)-(-)-1-amino-2-indolol;1-amino-2-indolol,(1S,2R)-(-)-amino-indolol
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CAS Number 126456-43-7

science Other reagents with same CAS 126456-43-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 149.19 g/mol
Formula C₉H₁₁NO
badge Registry Numbers
MDL Number MFCD00216655
thermostat Physical Properties
Melting Point 118-121 °C(lit.)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of protease inhibitors such as HIV-1 protease inhibitors. Its rigid indane structure and defined stereochemistry make it ideal for asymmetric synthesis, where it helps control the spatial arrangement of atoms in drug molecules. Commonly employed in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Also utilized in the preparation of catalysts for enantioselective reactions. Its amine group allows for easy incorporation into larger molecular frameworks through amide or sulfonamide bond formation.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿168.00
inventory 1g
10-20 days ฿180.00
inventory 5g
10-20 days ฿380.00
inventory 25g
10-20 days ฿1,750.00
inventory 100g
10-20 days ฿6,680.00

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(1S,2R)-(-)-cis-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 such as HIV-1 protease inhibitors. Its rigid indane structure and defined stereochemistry make it ideal for asymmetric synthesis, where it helps control the spatial arrangement of atoms in drug molecules. Commonly employed in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Also utilized in the preparation of catalysts for enantioselecti

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of protease inhibitors such as HIV-1 protease inhibitors. Its rigid indane structure and defined stereochemistry make it ideal for asymmetric synthesis, where it helps control the spatial arrangement of atoms in drug molecules. Commonly employed in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Also utilized in the preparation of catalysts for enantioselective reactions. Its amine group allows for easy incorporation into larger molecular frameworks through amide or sulfonamide bond formation.

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