5-Nitrobenzo[d]oxazol-2(3H)-one

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Reagent Code: #218913
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CAS Number 3889-13-2

science Other reagents with same CAS 3889-13-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 180.12 g/mol
Formula C₇H₄N₂O₄
badge Registry Numbers
MDL Number MFCD01929029
thermostat Physical Properties
Melting Point 242 °C
inventory_2 Storage & Handling
Density 1.580±0.06 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of fluorescent dyes and optical brighteners due to its nitro-aromatic structure and heterocyclic core. Its electron-withdrawing nitro group enhances reactivity in nucleophilic substitution, making it valuable in the preparation of bioactive molecules and agrochemicals. Also explored in the development of sensors for metal ions, leveraging its ability to undergo intramolecular charge transfer upon binding. Shows potential in medicinal chemistry as a scaffold for antimicrobial and anti-inflammatory agents, particularly in research settings focused on heterocyclic drug design.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿730.00
inventory 25g
10-20 days ฿9,480.00
inventory 100g
10-20 days ฿27,720.00
inventory 5g
10-20 days ฿2,500.00

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5-Nitrobenzo[d]oxazol-2(3H)-one
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Used as an intermediate in the synthesis of fluorescent dyes and optical brighteners due to its nitro-aromatic structure and heterocyclic core. Its electron-withdrawing nitro group enhances reactivity in nucleophilic substitution, making it valuable in the preparation of bioactive molecules and agrochemicals. Also explored in the development of sensors for metal ions, leveraging its ability to undergo intramolecular charge transfer upon binding. Shows potential in medicinal chemistry as a scaffold for an

Used as an intermediate in the synthesis of fluorescent dyes and optical brighteners due to its nitro-aromatic structure and heterocyclic core. Its electron-withdrawing nitro group enhances reactivity in nucleophilic substitution, making it valuable in the preparation of bioactive molecules and agrochemicals. Also explored in the development of sensors for metal ions, leveraging its ability to undergo intramolecular charge transfer upon binding. Shows potential in medicinal chemistry as a scaffold for antimicrobial and anti-inflammatory agents, particularly in research settings focused on heterocyclic drug design.

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