2-Bromo-6-hydroxypyridine

98%

Reagent Code: #144330
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CAS Number 27992-32-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 174.00 g/mol
Formula C₅H₄BrNO
badge Registry Numbers
MDL Number MFCD00234043
thermostat Physical Properties
Melting Point 121-125 °C
Boiling Point 336.6±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.776±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry, light-proof

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs targeting central nervous system disorders. It serves as a building block in the preparation of pyridine-based compounds with biological activity. Commonly employed in the manufacture of agrochemicals, including herbicides and fungicides, due to its ability to enhance molecular selectivity. Also utilized in research for the development of novel organic materials and catalysts. Its bromo and hydroxy functional groups allow for selective modifications, making it valuable in cross-coupling reactions and heterocyclic chemistry.

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Test Parameter Specification
Appearance White to Light Yellow to Purple Powder or Crystals
Purity 97.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿180.00
inventory 5g
10-20 days ฿750.00
inventory 25g
10-20 days ฿2,990.00
inventory 100g
10-20 days ฿7,210.00
2-Bromo-6-hydroxypyridine
Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs targeting central nervous system disorders. It serves as a building block in the preparation of pyridine-based compounds with biological activity. Commonly employed in the manufacture of agrochemicals, including herbicides and fungicides, due to its ability to enhance molecular selectivity. Also utilized in research for the development of novel organic materials and catalysts. Its bromo and hydroxy functional groups allow for selective modifications, making it valuable in cross-coupling reactions and heterocyclic chemistry.
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