2-Bromo-4-nitrophenol

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Reagent Code: #144761
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CAS Number 5847-59-6

science Other reagents with same CAS 5847-59-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 218.01 g/mol
Formula C₆H₄BrNO₃
badge Registry Numbers
MDL Number MFCD06656567
thermostat Physical Properties
Melting Point 111-115 °C
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of dyes, pharmaceuticals, and agrochemicals. It serves in the preparation of azo dyes due to its nitro and phenolic functionalities, which allow for diazotization and coupling reactions. Also employed in the development of certain antimicrobial agents and as a building block in organic synthesis for introducing bromo and nitro groups into more complex molecules. Its reactivity makes it valuable in cross-coupling reactions, particularly in research settings for creating novel aromatic compounds.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿300.00
inventory 5g
10-20 days ฿520.00
inventory 25g
10-20 days ฿2,150.00
inventory 100g
10-20 days ฿7,670.00

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2-Bromo-4-nitrophenol
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Used as an intermediate in the synthesis of dyes, pharmaceuticals, and agrochemicals. It serves in the preparation of azo dyes due to its nitro and phenolic functionalities, which allow for diazotization and coupling reactions. Also employed in the development of certain antimicrobial agents and as a building block in organic synthesis for introducing bromo and nitro groups into more complex molecules. Its reactivity makes it valuable in cross-coupling reactions, particularly in research settings for cre

Used as an intermediate in the synthesis of dyes, pharmaceuticals, and agrochemicals. It serves in the preparation of azo dyes due to its nitro and phenolic functionalities, which allow for diazotization and coupling reactions. Also employed in the development of certain antimicrobial agents and as a building block in organic synthesis for introducing bromo and nitro groups into more complex molecules. Its reactivity makes it valuable in cross-coupling reactions, particularly in research settings for creating novel aromatic compounds.

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