Pyridine,3-bromo-5-methoxy-, 1-oxide

≥95%

Reagent Code: #227120
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CAS Number 78156-39-5

science Other reagents with same CAS 78156-39-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 204.02 g/mol
Formula C₆H₆BrNO₂
badge Registry Numbers
MDL Number MFCD00234175
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules where the pyridine ring enhances binding affinity. The bromo and methoxy groups allow for further functionalization through cross-coupling reactions, making it valuable in medicinal chemistry for building complex heterocyclic systems. The N-oxide moiety increases solubility and can direct regioselective substitution, beneficial in optimizing reaction pathways during drug discovery. Also employed in the preparation of ligands for catalysis and in materials science for designing functional organic materials.

Available Sizes & Pricing

Size Availability Unit Price Quantity
500mg
10-20 days ฿11,300.00
1g
10-20 days ฿21,200.00
5g
10-20 days ฿45,550.00
Pyridine,3-bromo-5-methoxy-, 1-oxide
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules where the pyridine ring enhances binding affinity. The bromo and methoxy groups allow for further functionalization through cross-coupling reactions, making it valuable in medicinal chemistry for building complex heterocyclic systems. The N-oxide moiety increases solubility and can direct regioselective substitution, beneficial in optimizing reaction pathways during drug d

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules where the pyridine ring enhances binding affinity. The bromo and methoxy groups allow for further functionalization through cross-coupling reactions, making it valuable in medicinal chemistry for building complex heterocyclic systems. The N-oxide moiety increases solubility and can direct regioselective substitution, beneficial in optimizing reaction pathways during drug discovery. Also employed in the preparation of ligands for catalysis and in materials science for designing functional organic materials.

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