N-(2-Hydroxy-4-nitrophenyl)acetamide

95%

Reagent Code: #218918
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CAS Number 25351-89-7

science Other reagents with same CAS 25351-89-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 196.16 g/mol
Formula C₈H₈N₂O₄
badge Registry Numbers
MDL Number MFCD00219839
thermostat Physical Properties
Melting Point 258-259 °C
Boiling Point 436.1±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.477±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in the synthesis of dyes and pharmaceuticals. It serves in the development of azo dyes due to its aromatic nitro group and phenolic functionality, which are key for diazotization and coupling reactions. Also found application in the preparation of analgesic and antipyretic compounds, leveraging its structural similarity to paracetamol. Employed in research for developing nitroaromatic-based sensors and bioactive molecules.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,550.00
inventory 1g
10-20 days ฿3,150.00
inventory 5g
10-20 days ฿10,200.00
N-(2-Hydroxy-4-nitrophenyl)acetamide
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Used as an intermediate in the synthesis of dyes and pharmaceuticals. It serves in the development of azo dyes due to its aromatic nitro group and phenolic functionality, which are key for diazotization and coupling reactions. Also found application in the preparation of analgesic and antipyretic compounds, leveraging its structural similarity to paracetamol. Employed in research for developing nitroaromatic-based sensors and bioactive molecules.

Used as an intermediate in the synthesis of dyes and pharmaceuticals. It serves in the development of azo dyes due to its aromatic nitro group and phenolic functionality, which are key for diazotization and coupling reactions. Also found application in the preparation of analgesic and antipyretic compounds, leveraging its structural similarity to paracetamol. Employed in research for developing nitroaromatic-based sensors and bioactive molecules.

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