6-Nitroquinoxalin-5-amine

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Reagent Code: #214810
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CAS Number 57436-91-6

science Other reagents with same CAS 57436-91-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 190.16 g/mol
Formula C₈H₆N₄O₂
badge Registry Numbers
MDL Number MFCD21339783
inventory_2 Storage & Handling
Storage Room temperature, light-proof, inert gas

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in the development of antiviral, antibacterial, and anticancer agents. Exhibits potential in research for bioactive quinoxaline derivatives due to its nitro and amine functional groups, which allow for further chemical modifications. Derivatives demonstrate activity against Mycobacterium tuberculosis, the causative agent of tuberculosis, and in medications targeting the respiratory system. Also explored in the design of fluorescent probes and sensors owing to its electron-deficient aromatic structure. Shows promise in agrochemical research for developing novel pesticides with improved efficacy. The modifiable structure enables enhancements in potency while reducing toxicity to normal cells.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿9,150.00
5g
10-20 days ฿32,000.00
6-Nitroquinoxalin-5-amine
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Used in the synthesis of pharmaceutical intermediates, particularly in the development of antiviral, antibacterial, and anticancer agents. Exhibits potential in research for bioactive quinoxaline derivatives due to its nitro and amine functional groups, which allow for further chemical modifications. Derivatives demonstrate activity against Mycobacterium tuberculosis, the causative agent of tuberculosis, and in medications targeting the respiratory system. Also explored in the design of fluorescen

Used in the synthesis of pharmaceutical intermediates, particularly in the development of antiviral, antibacterial, and anticancer agents. Exhibits potential in research for bioactive quinoxaline derivatives due to its nitro and amine functional groups, which allow for further chemical modifications. Derivatives demonstrate activity against Mycobacterium tuberculosis, the causative agent of tuberculosis, and in medications targeting the respiratory system. Also explored in the design of fluorescent probes and sensors owing to its electron-deficient aromatic structure. Shows promise in agrochemical research for developing novel pesticides with improved efficacy. The modifiable structure enables enhancements in potency while reducing toxicity to normal cells.

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