4-Nitro-1-isoquinolinamine

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Reagent Code: #219157
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CAS Number 78886-54-1

science Other reagents with same CAS 78886-54-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 189.17 g/mol
Formula C₉H₇N₃O₂
badge Registry Numbers
MDL Number MFCD18448266
inventory_2 Storage & Handling
Density 1.445 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in the development of kinase inhibitors and anticancer agents. Its structure serves as a building block in medicinal chemistry for constructing nitrogen-containing heterocyclic compounds. Commonly employed in research settings to design bioactive molecules due to the electron-withdrawing nitro group enhancing reactivity for further functionalization. Also utilized in the preparation of fluorescent probes and sensors owing to its aromatic and amine properties that support conjugation and signal detection.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,430.00
inventory 250mg
10-20 days ฿15,330.00
inventory 1g
10-20 days ฿29,740.00

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4-Nitro-1-isoquinolinamine
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Used in the synthesis of pharmaceutical intermediates, particularly in the development of kinase inhibitors and anticancer agents. Its structure serves as a building block in medicinal chemistry for constructing nitrogen-containing heterocyclic compounds. Commonly employed in research settings to design bioactive molecules due to the electron-withdrawing nitro group enhancing reactivity for further functionalization. Also utilized in the preparation of fluorescent probes and sensors owing to its aromatic

Used in the synthesis of pharmaceutical intermediates, particularly in the development of kinase inhibitors and anticancer agents. Its structure serves as a building block in medicinal chemistry for constructing nitrogen-containing heterocyclic compounds. Commonly employed in research settings to design bioactive molecules due to the electron-withdrawing nitro group enhancing reactivity for further functionalization. Also utilized in the preparation of fluorescent probes and sensors owing to its aromatic and amine properties that support conjugation and signal detection.

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