3-Methoxyisoquinolin-7-amine

95%

Reagent Code: #210027
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CAS Number 1374652-58-0

science Other reagents with same CAS 1374652-58-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 174.2 g/mol
Formula C₁₀H₁₀N₂O
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MDL Number MFCD22380559
inventory_2 Storage & Handling
Storage 2-8°C, inflatable, light-proof

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Used in pharmaceutical research as a key intermediate in the synthesis of bioactive compounds, particularly in the development of central nervous system agents and kinase inhibitors. Shows potential in the design of novel therapeutics targeting neurological disorders due to its structural affinity with isoquinoline-based neurotransmitters. Also employed in the preparation of fluorescent probes for biochemical assays, leveraging its luminescent properties when derivatized. Its amine functionality allows for easy conjugation, making it valuable in medicinal chemistry for structure-activity relationship studies.

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inventory 1g
10-20 days ฿46,800.00

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3-Methoxyisoquinolin-7-amine
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Used in pharmaceutical research as a key intermediate in the synthesis of bioactive compounds, particularly in the development of central nervous system agents and kinase inhibitors. Shows potential in the design of novel therapeutics targeting neurological disorders due to its structural affinity with isoquinoline-based neurotransmitters. Also employed in the preparation of fluorescent probes for biochemical assays, leveraging its luminescent properties when derivatized. Its amine functionality allows f

Used in pharmaceutical research as a key intermediate in the synthesis of bioactive compounds, particularly in the development of central nervous system agents and kinase inhibitors. Shows potential in the design of novel therapeutics targeting neurological disorders due to its structural affinity with isoquinoline-based neurotransmitters. Also employed in the preparation of fluorescent probes for biochemical assays, leveraging its luminescent properties when derivatized. Its amine functionality allows for easy conjugation, making it valuable in medicinal chemistry for structure-activity relationship studies.

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