Methyl 4-aminoquinoline-8-carboxylate hydrochloride

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Reagent Code: #47023
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CAS Number 1447608-03-8

science Other reagents with same CAS 1447608-03-8

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Weight 238.67 g/mol
Formula C₁₁H₁₁ClN₂O₂
badge Registry Numbers
MDL Number MFCD25541922
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description Product Description

Used primarily in pharmaceutical research, this compound serves as a key intermediate in the synthesis of various quinoline-based drugs. Its structure is particularly valuable in developing antimalarial agents, leveraging the quinoline core known for its efficacy against malaria parasites. Additionally, it finds application in the study of potential anticancer compounds, where its derivatives are explored for their ability to inhibit specific cellular pathways. Researchers also utilize it in organic synthesis to create complex molecules for further biological testing. Its hydrochloride form enhances solubility, making it more suitable for experimental procedures in aqueous environments.

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inventory 100mg
10-20 days ฿13,400.00

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Methyl 4-aminoquinoline-8-carboxylate hydrochloride
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Used primarily in pharmaceutical research, this compound serves as a key intermediate in the synthesis of various quinoline-based drugs. Its structure is particularly valuable in developing antimalarial agents, leveraging the quinoline core known for its efficacy against malaria parasites. Additionally, it finds application in the study of potential anticancer compounds, where its derivatives are explored for their ability to inhibit specific cellular pathways. Researchers also utilize it in organic synt

Used primarily in pharmaceutical research, this compound serves as a key intermediate in the synthesis of various quinoline-based drugs. Its structure is particularly valuable in developing antimalarial agents, leveraging the quinoline core known for its efficacy against malaria parasites. Additionally, it finds application in the study of potential anticancer compounds, where its derivatives are explored for their ability to inhibit specific cellular pathways. Researchers also utilize it in organic synthesis to create complex molecules for further biological testing. Its hydrochloride form enhances solubility, making it more suitable for experimental procedures in aqueous environments.

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