4-(1H-Benzo[d]imidazol-2-yl)-1,2,5-oxadiazol-3-amine

98%

Reagent Code: #196307
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CAS Number 332026-86-5

science Other reagents with same CAS 332026-86-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 201.18 g/mol
Formula C₉H₇N₅O
badge Registry Numbers
MDL Number MFCD00501862
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Used in medicinal chemistry as a key scaffold in the development of kinase inhibitors and anti-inflammatory agents. Its structure supports binding to enzyme active sites, particularly in proteins involved in cell signaling pathways. It is also explored in the design of antiviral and anticancer compounds due to its ability to mimic purine-like motifs in biological systems. Additionally, this compound serves as an intermediate in synthesizing fluorescent probes for biochemical imaging, leveraging its electron-rich heterocyclic core for optical applications.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿770.00
1g
10-20 days ฿2,030.00
5g
10-20 days ฿6,890.00
4-(1H-Benzo[d]imidazol-2-yl)-1,2,5-oxadiazol-3-amine
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Used in medicinal chemistry as a key scaffold in the development of kinase inhibitors and anti-inflammatory agents. Its structure supports binding to enzyme active sites, particularly in proteins involved in cell signaling pathways. It is also explored in the design of antiviral and anticancer compounds due to its ability to mimic purine-like motifs in biological systems. Additionally, this compound serves as an intermediate in synthesizing fluorescent probes for biochemical imaging, leveraging its elect

Used in medicinal chemistry as a key scaffold in the development of kinase inhibitors and anti-inflammatory agents. Its structure supports binding to enzyme active sites, particularly in proteins involved in cell signaling pathways. It is also explored in the design of antiviral and anticancer compounds due to its ability to mimic purine-like motifs in biological systems. Additionally, this compound serves as an intermediate in synthesizing fluorescent probes for biochemical imaging, leveraging its electron-rich heterocyclic core for optical applications.

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