2-Amino-7-methoxy-1H-benzo[d]imidazole-5-carboxylicacid

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Reagent Code: #139450
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CAS Number 2172017-91-1

science Other reagents with same CAS 2172017-91-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 207.19 g/mol
Formula C₉H₉N₃O₃
inventory_2 Storage & Handling
Storage 2-8°C

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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and anticancer agents. Its structure supports the formation of biologically active molecules by serving as a building block in heterocyclic chemistry. Commonly employed in medicinal chemistry for designing kinase inhibitors and other targeted therapies. Also utilized in research settings to develop fluorescent probes due to its ability to form stable derivatives with detectable emission properties. Its carboxylic acid and amino groups allow for easy functionalization, making it valuable in combinatorial chemistry and drug discovery.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿17,500.00

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2-Amino-7-methoxy-1H-benzo[d]imidazole-5-carboxylicacid
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and anticancer agents. Its structure supports the formation of biologically active molecules by serving as a building block in heterocyclic chemistry. Commonly employed in medicinal chemistry for designing kinase inhibitors and other targeted therapies. Also utilized in research settings to develop fluorescent probes due to its ability to form stable derivatives with detectable emission properties

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and anticancer agents. Its structure supports the formation of biologically active molecules by serving as a building block in heterocyclic chemistry. Commonly employed in medicinal chemistry for designing kinase inhibitors and other targeted therapies. Also utilized in research settings to develop fluorescent probes due to its ability to form stable derivatives with detectable emission properties. Its carboxylic acid and amino groups allow for easy functionalization, making it valuable in combinatorial chemistry and drug discovery.

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