(R)-1-(5-Bromopyridin-2-yl)ethanamine

95%

Reagent Code: #231054
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CAS Number 953780-20-6

science Other reagents with same CAS 953780-20-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 201.066 g/mol
Formula C₇H₉BrN₂
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for targeted cancer therapies. Its enantiomeric purity is critical for optimal biological activity and selectivity in drug candidates. Commonly employed in the preparation of active pharmaceutical ingredients (APIs) where the (R)-configuration enhances binding affinity to specific enzyme targets. Also utilized in research settings for the construction of nitrogen-containing heterocyclic compounds with potential neuroactive or anti-inflammatory properties.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿13,590.00
inventory 250mg
10-20 days ฿32,570.00
inventory 100mg
10-20 days ฿24,110.00
(R)-1-(5-Bromopyridin-2-yl)ethanamine
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Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for targeted cancer therapies. Its enantiomeric purity is critical for optimal biological activity and selectivity in drug candidates. Commonly employed in the preparation of active pharmaceutical ingredients (APIs) where the (R)-configuration enhances binding affinity to specific enzyme targets. Also utilized in research settings for the construction of nitrogen-containing heterocy

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for targeted cancer therapies. Its enantiomeric purity is critical for optimal biological activity and selectivity in drug candidates. Commonly employed in the preparation of active pharmaceutical ingredients (APIs) where the (R)-configuration enhances binding affinity to specific enzyme targets. Also utilized in research settings for the construction of nitrogen-containing heterocyclic compounds with potential neuroactive or anti-inflammatory properties.

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