2-Hydroxy-5-nitrobenzamide

≥95%

Reagent Code: #195597
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CAS Number 2912-78-9

science Other reagents with same CAS 2912-78-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 182.13 g/mol
Formula C₇H₆N₂O₄
badge Registry Numbers
MDL Number MFCD12027045
thermostat Physical Properties
Boiling Point 357.6°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, away from light, stored in inert gas

description Product Description

Used as an intermediate in the synthesis of dyes and pharmaceuticals, particularly in the development of compounds with biological activity. It serves in the preparation of heterocyclic derivatives due to the presence of both hydroxyl and amide functional groups, which allow for further chemical modifications. Commonly employed in research settings for the development of nitroaromatic compounds with potential antimicrobial or anti-inflammatory properties. Also utilized in analytical chemistry as a reagent for the detection of certain metal ions owing to its ability to form colored complexes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,800.00
inventory 250mg
10-20 days ฿2,690.00
inventory 1g
10-20 days ฿6,760.00
inventory 5g
10-20 days ฿18,880.00

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2-Hydroxy-5-nitrobenzamide
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Used as an intermediate in the synthesis of dyes and pharmaceuticals, particularly in the development of compounds with biological activity. It serves in the preparation of heterocyclic derivatives due to the presence of both hydroxyl and amide functional groups, which allow for further chemical modifications. Commonly employed in research settings for the development of nitroaromatic compounds with potential antimicrobial or anti-inflammatory properties. Also utilized in analytical chemistry as a reagen

Used as an intermediate in the synthesis of dyes and pharmaceuticals, particularly in the development of compounds with biological activity. It serves in the preparation of heterocyclic derivatives due to the presence of both hydroxyl and amide functional groups, which allow for further chemical modifications. Commonly employed in research settings for the development of nitroaromatic compounds with potential antimicrobial or anti-inflammatory properties. Also utilized in analytical chemistry as a reagent for the detection of certain metal ions owing to its ability to form colored complexes.

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