2,3-Dichloro-6-nitroquinoxaline

≥98%

Reagent Code: #174367
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CAS Number 2379-60-4

science Other reagents with same CAS 2379-60-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 244.03 g/mol
Formula C₈H₃Cl₂N₃O₂
badge Registry Numbers
MDL Number MFCD00454905
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals, this compound plays a key role in constructing quinoxaline-based derivatives with biological activity. Its electrophilic sites allow for selective substitutions, making it valuable in developing kinase inhibitors and antimicrobial agents. It is also employed in materials science for creating electron-deficient aromatic systems used in organic semiconductors and fluorescent probes. Due to the presence of nitro and halogen groups, it serves as a building block in cross-coupling reactions, facilitating the development of complex heterocyclic compounds for research and industrial applications.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿176.00
inventory 1g
10-20 days ฿544.50
inventory 5g
10-20 days ฿2,315.50

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2,3-Dichloro-6-nitroquinoxaline
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Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals, this compound plays a key role in constructing quinoxaline-based derivatives with biological activity. Its electrophilic sites allow for selective substitutions, making it valuable in developing kinase inhibitors and antimicrobial agents. It is also employed in materials science for creating electron-deficient aromatic systems used in organic semiconductors and fluorescent probes. Due to the presence of nitro and hal

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals, this compound plays a key role in constructing quinoxaline-based derivatives with biological activity. Its electrophilic sites allow for selective substitutions, making it valuable in developing kinase inhibitors and antimicrobial agents. It is also employed in materials science for creating electron-deficient aromatic systems used in organic semiconductors and fluorescent probes. Due to the presence of nitro and halogen groups, it serves as a building block in cross-coupling reactions, facilitating the development of complex heterocyclic compounds for research and industrial applications.

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