(1S,2R)-1-Amino-6-bromo-2,3-dihydro-1H-inden-2-ol

95%

Reagent Code: #233186
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CAS Number 2412424-43-0

science Other reagents with same CAS 2412424-43-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 228.09 g/mol
Formula C₉H₁₀BrNO
thermostat Physical Properties
Boiling Point 325.6±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.637±0.06 g/cm3(Predicted)
Storage Room temperature, light-proof, inert gas

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of serotonin and norepinephrine reuptake inhibitors. Its stereochemistry enables selective biological activity, making it valuable in creating enantiomerically pure drugs for treating neurological and psychiatric disorders such as depression and anxiety. Commonly employed in asymmetric synthesis routes due to its stable chiral scaffold and functional group compatibility.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿12,980.00
inventory 1g
10-20 days ฿34,580.00
inventory 5g
10-20 days ฿115,230.00
(1S,2R)-1-Amino-6-bromo-2,3-dihydro-1H-inden-2-ol
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Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of serotonin and norepinephrine reuptake inhibitors. Its stereochemistry enables selective biological activity, making it valuable in creating enantiomerically pure drugs for treating neurological and psychiatric disorders such as depression and anxiety. Commonly employed in asymmetric synthesis routes due to its stable chiral scaffold and functional group compatibility.

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of serotonin and norepinephrine reuptake inhibitors. Its stereochemistry enables selective biological activity, making it valuable in creating enantiomerically pure drugs for treating neurological and psychiatric disorders such as depression and anxiety. Commonly employed in asymmetric synthesis routes due to its stable chiral scaffold and functional group compatibility.

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