Methyl 5-bromo-2-chloro-1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylate

≥95%

Reagent Code: #120125
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CAS Number 869357-63-1

science Other reagents with same CAS 869357-63-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 280.50 g/mol
Formula C₈H₇BrClNO₃
badge Registry Numbers
MDL Number MFCD26395170
thermostat Physical Properties
Boiling Point 306.6±42.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This compound is primarily utilized in the field of organic synthesis, where it serves as a versatile intermediate for the development of more complex molecules. Its structure, featuring both bromo and chloro substituents, makes it particularly valuable in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, which are essential in the construction of pharmaceuticals and agrochemicals. Additionally, the presence of the ester group allows for further functionalization through hydrolysis or transesterification, enabling the synthesis of carboxylic acids or other ester derivatives. Researchers also leverage this compound in the preparation of heterocyclic compounds, which are often key components in drug discovery and material science. Its reactivity and stability make it a useful building block in medicinal chemistry for designing biologically active molecules.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,671.00
inventory 100mg
10-20 days ฿2,331.00

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Methyl 5-bromo-2-chloro-1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylate
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This compound is primarily utilized in the field of organic synthesis, where it serves as a versatile intermediate for the development of more complex molecules. Its structure, featuring both bromo and chloro substituents, makes it particularly valuable in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, which are essential in the construction of pharmaceuticals and agrochemicals. Additionally, the presence of the ester group allows for further functionalization through hydrolysis or transesterification, enabling the synthesis of carboxylic acids or other ester derivatives. Researchers also leverage this compound in the preparation of heterocyclic compounds, which are often key components in drug discovery and material science. Its reactivity and stability make it a useful building block in medicinal chemistry for designing biologically active molecules.
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