2-Bromo-5-nitrophenol

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Reagent Code: #143496
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CAS Number 52427-05-1

science Other reagents with same CAS 52427-05-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 218.00 g/mol
Formula C₆H₄BrNO₃
badge Registry Numbers
MDL Number MFCD00466299
thermostat Physical Properties
Melting Point 116-121 °C
Boiling Point 278.8 °C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, light-proof, inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the preparation of dyes and fungicides. It serves as a building block in organic reactions where bromo and nitro functional groups allow for further substitution and transformation. Commonly applied in research settings for developing new bioactive compounds due to its reactivity in coupling reactions and nucleophilic substitutions. Also utilized in the production of certain photochromic materials and UV absorbers in specialty polymers.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,170.00
inventory 25g
10-20 days ฿5,800.00
inventory 100g
10-20 days ฿23,120.00

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2-Bromo-5-nitrophenol
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the preparation of dyes and fungicides. It serves as a building block in organic reactions where bromo and nitro functional groups allow for further substitution and transformation. Commonly applied in research settings for developing new bioactive compounds due to its reactivity in coupling reactions and nucleophilic substitutions. Also utilized in the production of certain photochromic materials and UV absorb

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the preparation of dyes and fungicides. It serves as a building block in organic reactions where bromo and nitro functional groups allow for further substitution and transformation. Commonly applied in research settings for developing new bioactive compounds due to its reactivity in coupling reactions and nucleophilic substitutions. Also utilized in the production of certain photochromic materials and UV absorbers in specialty polymers.

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