(R)-1-(5-Chloropyridin-3-yl)ethanamine

95%

Reagent Code: #230962
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CAS Number 1213144-64-9

science Other reagents with same CAS 1213144-64-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 156.61 g/mol
Formula C₇H₉ClN₂
badge Registry Numbers
MDL Number MFCD11008089
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 production of selective kinase inhibitors and neuroactive compounds. Its enantiomeric purity is critical for achieving desired biological activity in drug candidates targeting central nervous system disorders and inflammatory diseases. Commonly employed in asymmetric synthesis routes where the (R)-configuration enhances binding affinity and metabolic stability. Also utilized in agrochemicals for developing bioactive molecules with improved environmental selectivity.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿13,140.00
inventory 100mg
10-20 days ฿15,780.00
inventory 250mg
10-20 days ฿25,560.00

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(R)-1-(5-Chloropyridin-3-yl)ethanamine
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Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of selective kinase inhibitors and neuroactive compounds. Its enantiomeric purity is critical for achieving desired biological activity in drug candidates targeting central nervous system disorders and inflammatory diseases. Commonly employed in asymmetric synthesis routes where the (R)-configuration enhances binding affinity and metabolic stability. Also utilized in agrochemicals for developing bioactiv

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of selective kinase inhibitors and neuroactive compounds. Its enantiomeric purity is critical for achieving desired biological activity in drug candidates targeting central nervous system disorders and inflammatory diseases. Commonly employed in asymmetric synthesis routes where the (R)-configuration enhances binding affinity and metabolic stability. Also utilized in agrochemicals for developing bioactive molecules with improved environmental selectivity.

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