2-Bromo-6-methylpyridine 1-oxide

94%

Reagent Code: #142422
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CAS Number 91668-84-7

science Other reagents with same CAS 91668-84-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 188.02 g/mol
Formula C₆H₆BrNO
badge Registry Numbers
MDL Number MFCD26704648
inventory_2 Storage & Handling
Storage 2-8 °C, sealed, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor ligands and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating analogs with potential neurological activity. Also employed in agrochemical research for designing novel pesticides and herbicides due to its stability and reactivity in coupling reactions. The N-oxide group enhances solubility and directs regioselective substitution, which is advantageous in multi-step organic synthesis.

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Test Parameter Specification
Appearance Light yellow Solid
Purity (%) 93.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿11,520.00
inventory 1g
10-20 days ฿34,560.00
inventory 100mg
10-20 days ฿6,120.00

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2-Bromo-6-methylpyridine 1-oxide
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor ligands and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating analogs with potential neurological activity. Also employed in agrochemical research for designing novel pesticides and herbicides due to its stability and reactivity in coupling reactions. The N-oxide group enhances solubility and directs regios

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic receptor ligands and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating analogs with potential neurological activity. Also employed in agrochemical research for designing novel pesticides and herbicides due to its stability and reactivity in coupling reactions. The N-oxide group enhances solubility and directs regioselective substitution, which is advantageous in multi-step organic synthesis.

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