6-Nitro-1H-benzo[d]imidazol-2-amine

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Reagent Code: #217302
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CAS Number 6232-92-4

science Other reagents with same CAS 6232-92-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 178.15 g/mol
Formula C₇H₆N₄O₂
badge Registry Numbers
MDL Number MFCD06659794
thermostat Physical Properties
Boiling Point 478.5°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antiparasitic and antiviral agents. Its structure supports the design of compounds that can interact with biological targets such as enzymes and receptors. Commonly employed in research settings for the preparation of benzimidazole derivatives, which are known for their broad biological activity. Also utilized in the creation of fluorescent probes for biochemical assays due to its electron-withdrawing nitro group and amine functionality. Shows potential in agrochemical research for developing new classes of pesticides and herbicides.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,680.00
inventory 5g
10-20 days ฿5,560.00

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6-Nitro-1H-benzo[d]imidazol-2-amine
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antiparasitic and antiviral agents. Its structure supports the design of compounds that can interact with biological targets such as enzymes and receptors. Commonly employed in research settings for the preparation of benzimidazole derivatives, which are known for their broad biological activity. Also utilized in the creation of fluorescent probes for biochemical assays due to its electron-withdrawing nitro gr

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antiparasitic and antiviral agents. Its structure supports the design of compounds that can interact with biological targets such as enzymes and receptors. Commonly employed in research settings for the preparation of benzimidazole derivatives, which are known for their broad biological activity. Also utilized in the creation of fluorescent probes for biochemical assays due to its electron-withdrawing nitro group and amine functionality. Shows potential in agrochemical research for developing new classes of pesticides and herbicides.

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