Methyl 2-(3-bromopyridin-4-yl)acetate

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Reagent Code: #58594
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CAS Number 162615-12-5

science Other reagents with same CAS 162615-12-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 230.0586 g/mol
Formula C₈H₈BrNO₂
badge Registry Numbers
MDL Number MFCD10000071
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

This chemical is primarily used in organic synthesis as a key intermediate for the development of various pharmaceuticals and agrochemicals. Its structure, featuring a bromopyridine moiety, makes it valuable for constructing complex molecules, particularly in the synthesis of active pharmaceutical ingredients (APIs). It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce functional groups or build heterocyclic frameworks. Additionally, it serves as a precursor in the production of compounds with potential biological activities, including antimicrobial, antiviral, or anticancer properties. Its ester group also allows for further chemical modifications, making it versatile in medicinal chemistry and drug discovery processes.

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Test Parameter Specification
Appearance Yellow Liquid
Purity (%) 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,000.00
inventory 250mg
10-20 days ฿15,300.00
inventory 1g
10-20 days ฿38,700.00

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Methyl 2-(3-bromopyridin-4-yl)acetate
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This chemical is primarily used in organic synthesis as a key intermediate for the development of various pharmaceuticals and agrochemicals. Its structure, featuring a bromopyridine moiety, makes it valuable for constructing complex molecules, particularly in the synthesis of active pharmaceutical ingredients (APIs). It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce functional groups or build heterocyclic frameworks. Additionally, it serves as a

This chemical is primarily used in organic synthesis as a key intermediate for the development of various pharmaceuticals and agrochemicals. Its structure, featuring a bromopyridine moiety, makes it valuable for constructing complex molecules, particularly in the synthesis of active pharmaceutical ingredients (APIs). It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce functional groups or build heterocyclic frameworks. Additionally, it serves as a precursor in the production of compounds with potential biological activities, including antimicrobial, antiviral, or anticancer properties. Its ester group also allows for further chemical modifications, making it versatile in medicinal chemistry and drug discovery processes.

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