1-(5-bromopyridin-2-yl)ethanone

95%

Reagent Code: #144207
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CAS Number 214701-49-2

science Other reagents with same CAS 214701-49-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 200.03 g/mol
Formula C₇H₆BrNO
badge Registry Numbers
MDL Number MFCD04974523
inventory_2 Storage & Handling
Storage Room temperature

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. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating drug candidates targeting cancer and inflammatory diseases. Commonly employed in cross-coupling reactions, such as Suzuki-Miyaura and Buchwald-Hartwig, to build complex heterocyclic systems found in modern therapeutics. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its reactivity and stability in various reaction conditions.

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Test Parameter Specification
Appearance White to Yellow Solid
Purity (%) 94.5-100
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿310.00
inventory 5g
10-20 days ฿1,120.00
inventory 25g
10-20 days ฿5,410.00
inventory 100g
10-20 days ฿20,840.00

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1-(5-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. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating drug candidates targeting cancer and inflammatory diseases. Commonly employed in cross-coupling reactions, such as Suzuki-Miyaura and Buchwald-Hartwig, to build complex heterocyclic systems found in modern therapeutics. Also utilized in agroc

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating drug candidates targeting cancer and inflammatory diseases. Commonly employed in cross-coupling reactions, such as Suzuki-Miyaura and Buchwald-Hartwig, to build complex heterocyclic systems found in modern therapeutics. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its reactivity and stability in various reaction conditions.

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