2-Bromo-1-(6-bromopyridin-2-yl)ethanone

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Reagent Code: #141049
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CAS Number 142978-11-8

science Other reagents with same CAS 142978-11-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 278.92 g/mol
Formula C₇H₅NOBr₂
badge Registry Numbers
MDL Number MFCD07785847
thermostat Physical Properties
Boiling Point 321.6±32.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.943±0.06 g/cm3(Predicted)
Storage 2-8°C, Inert Gas

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. The compound features two bromine atoms and a ketone group, enabling diverse reaction pathways such as nucleophilic substitutions and the formation of complex heterocyclic structures. Its structure allows for selective functionalization in multi-step reactions, making it valuable in medicinal chemistry. Commonly employed in cross-coupling reactions and heterocycle formation, it supports the construction of complex molecules for drug discovery. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its reactivity and ability to introduce bromine moieties into target frameworks.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿12,280.00
inventory 100mg
10-20 days ฿20,860.00

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2-Bromo-1-(6-bromopyridin-2-yl)ethanone
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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. The compound features two bromine atoms and a ketone group, enabling diverse reaction pathways such as nucleophilic substitutions and the formation of complex heterocyclic structures. Its structure allows for selective functionalization in multi-step reactions, making it valuable in medicinal chemistry. Commonly employed in cross-coupling reactions

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. The compound features two bromine atoms and a ketone group, enabling diverse reaction pathways such as nucleophilic substitutions and the formation of complex heterocyclic structures. Its structure allows for selective functionalization in multi-step reactions, making it valuable in medicinal chemistry. Commonly employed in cross-coupling reactions and heterocycle formation, it supports the construction of complex molecules for drug discovery. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its reactivity and ability to introduce bromine moieties into target frameworks.

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