6-Bromo-N-methylpyridin-3-amine

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Reagent Code: #150279
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CAS Number 1022641-52-6

science Other reagents with same CAS 1022641-52-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 187.04 g/mol
Formula C₆H₇BrN₂
badge Registry Numbers
MDL Number MFCD00234191
inventory_2 Storage & Handling
Storage 2-8°C, avoid light, inert gas storage

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in the preparation of biologically active compounds due to the presence of both bromine and amine functional groups, which allow for further chemical modifications through cross-coupling reactions and nucleophilic substitutions. Commonly employed in medicinal chemistry for structure-activity relationship studies to optimize drug candidates targeting neurological disorders and inflammatory diseases. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and selectivity.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,640.00
inventory 5g
10-20 days ฿7,010.00
inventory 25g
10-20 days ฿22,640.00

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6-Bromo-N-methylpyridin-3-amine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in the preparation of biologically active compounds due to the presence of both bromine and amine functional groups, which allow for further chemical modifications through cross-coupling reactions and nucleophilic substitutions. Commonly employed in medicinal chemistry for structure-activity relationship studies to optimize drug candidate

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in the preparation of biologically active compounds due to the presence of both bromine and amine functional groups, which allow for further chemical modifications through cross-coupling reactions and nucleophilic substitutions. Commonly employed in medicinal chemistry for structure-activity relationship studies to optimize drug candidates targeting neurological disorders and inflammatory diseases. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and selectivity.

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