3,5-Dibromo-2-pyridinol

98%

Reagent Code: #169679
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CAS Number 13472-81-6

science Other reagents with same CAS 13472-81-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 252.89 g/mol
Formula C₅H₃Br₂NO
badge Registry Numbers
EC Number 000-000-0
MDL Number MFCD00023472
thermostat Physical Properties
Melting Point 204-210 °C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fungicides and herbicides. It serves as a building block in the preparation of complex heterocyclic compounds due to its reactive halogen groups, which allow for further functionalization through cross-coupling reactions. Also employed in research for developing corrosion inhibitors and in the formulation of biocides for industrial water treatment. Its structural features make it valuable in medicinal chemistry for designing bioactive molecules targeting enzyme inhibition.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿143.00
5g
10-20 days ฿610.00
25g
10-20 days ฿1,628.00
100g
10-20 days ฿11,390.00

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3,5-Dibromo-2-pyridinol
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fungicides and herbicides. It serves as a building block in the preparation of complex heterocyclic compounds due to its reactive halogen groups, which allow for further functionalization through cross-coupling reactions. Also employed in research for developing corrosion inhibitors and in the formulation of biocides for industrial water treatment. Its structural features make it valuable in med
Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fungicides and herbicides. It serves as a building block in the preparation of complex heterocyclic compounds due to its reactive halogen groups, which allow for further functionalization through cross-coupling reactions. Also employed in research for developing corrosion inhibitors and in the formulation of biocides for industrial water treatment. Its structural features make it valuable in medicinal chemistry for designing bioactive molecules targeting enzyme inhibition.
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