5-Chloro-7-nitrobenzo[d]oxazol-2(3H)-one

95%

Reagent Code: #156627
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CAS Number 811810-67-0

science Other reagents with same CAS 811810-67-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.56 g/mol
Formula C₇H₃ClN₂O₄
badge Registry Numbers
MDL Number MFCD09753602
inventory_2 Storage & Handling
Density 1.704±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of fluorescent dyes and bioactive compounds, particularly in the development of optical brighteners and sensors. Its structure supports conjugation systems that enhance fluorescence properties, making it valuable in labeling biomolecules for imaging and detection in biological research. Also employed in the preparation of pharmaceuticals with antimicrobial and anti-inflammatory activities due to its electron-withdrawing substituents that influence drug-receptor interactions.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿5,850.00
250mg
10-20 days ฿9,910.00
1g
10-20 days ฿26,720.00
5-Chloro-7-nitrobenzo[d]oxazol-2(3H)-one
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Used as a key intermediate in the synthesis of fluorescent dyes and bioactive compounds, particularly in the development of optical brighteners and sensors. Its structure supports conjugation systems that enhance fluorescence properties, making it valuable in labeling biomolecules for imaging and detection in biological research. Also employed in the preparation of pharmaceuticals with antimicrobial and anti-inflammatory activities due to its electron-withdrawing substituents that influence drug-receptor

Used as a key intermediate in the synthesis of fluorescent dyes and bioactive compounds, particularly in the development of optical brighteners and sensors. Its structure supports conjugation systems that enhance fluorescence properties, making it valuable in labeling biomolecules for imaging and detection in biological research. Also employed in the preparation of pharmaceuticals with antimicrobial and anti-inflammatory activities due to its electron-withdrawing substituents that influence drug-receptor interactions.

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