5-Bromo-3-chloropyridin-2-amine

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Reagent Code: #145053
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CAS Number 38185-55-6

science Other reagents with same CAS 38185-55-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 207.46 g/mol
Formula C₅H₄BrClN₂
thermostat Physical Properties
Melting Point 94-96°C
Boiling Point 232.5°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. It serves as a building block in agrochemicals, contributing to the creation of pesticides and herbicides with improved efficacy. Its halogenated pyridine structure allows for selective cross-coupling reactions, making it valuable in medicinal chemistry for drug discovery and optimization. Also employed in research laboratories for the design of novel compounds with potential antiviral or anticancer properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,080.00
inventory 10g
10-20 days ฿2,020.00
inventory 25g
10-20 days ฿4,570.00
inventory 100g
10-20 days ฿15,690.00

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5-Bromo-3-chloropyridin-2-amine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. It serves as a building block in agrochemicals, contributing to the creation of pesticides and herbicides with improved efficacy. Its halogenated pyridine structure allows for selective cross-coupling reactions, making it valuable in medicinal chemistry for drug discovery and optimization. Also employed in research laboratories for the design of nov

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. It serves as a building block in agrochemicals, contributing to the creation of pesticides and herbicides with improved efficacy. Its halogenated pyridine structure allows for selective cross-coupling reactions, making it valuable in medicinal chemistry for drug discovery and optimization. Also employed in research laboratories for the design of novel compounds with potential antiviral or anticancer properties.

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