3,5-DINITRO-4-HYDROXYBENZOIC ACID

≥98%

Reagent Code: #168464
label
Alias 4-hydroxy-3,5-dinitrobenzoic acid
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CAS Number 1019-52-9

science Other reagents with same CAS 1019-52-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 228.12 g/mol
Formula C₇H₄N₂O₇
badge Registry Numbers
MDL Number MFCD00017000
thermostat Physical Properties
Melting Point 249-252 °C
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and dyes. It serves in the preparation of certain analgesic and anti-inflammatory compounds due to its functional groups that allow further chemical modifications. Also employed in research settings for developing novel organic compounds, particularly in the design of nitro-containing bioactive molecules. Its hydroxy and carboxylic acid groups enable salt formation and esterification, useful in prodrug strategies. Additionally, it finds use in analytical chemistry as a derivatizing agent for detecting amines and alcohols.

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inventory 1g
10-20 days ฿9,810.00

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3,5-DINITRO-4-HYDROXYBENZOIC ACID
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Used as an intermediate in the synthesis of pharmaceuticals and dyes. It serves in the preparation of certain analgesic and anti-inflammatory compounds due to its functional groups that allow further chemical modifications. Also employed in research settings for developing novel organic compounds, particularly in the design of nitro-containing bioactive molecules. Its hydroxy and carboxylic acid groups enable salt formation and esterification, useful in prodrug strategies. Additionally, it finds use in anal
Used as an intermediate in the synthesis of pharmaceuticals and dyes. It serves in the preparation of certain analgesic and anti-inflammatory compounds due to its functional groups that allow further chemical modifications. Also employed in research settings for developing novel organic compounds, particularly in the design of nitro-containing bioactive molecules. Its hydroxy and carboxylic acid groups enable salt formation and esterification, useful in prodrug strategies. Additionally, it finds use in analytical chemistry as a derivatizing agent for detecting amines and alcohols.
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