4,6-DIAMINO-2-METHYL-QUINOLINE

≥95%

Reagent Code: #43546
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CAS Number 5443-31-2

science Other reagents with same CAS 5443-31-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 173.21 g/mol
Formula C₁₀H₁₁N₃
thermostat Physical Properties
Melting Point 278℃ (decomp)
Boiling Point 411.7±40.0℃(Predicted)
inventory_2 Storage & Handling
Density 1.258±0.06 g/cm3(Predicted)
Storage 2-8℃, dry

description Product Description

Used primarily in the synthesis of pharmaceutical compounds, it serves as a key intermediate in the production of antimalarial drugs. Its structure is valuable in medicinal chemistry for developing molecules with potential therapeutic effects. Additionally, it is employed in research settings to study chemical reactions and mechanisms involving quinoline derivatives. Its applications extend to the development of dyes and pigments, where its chemical properties contribute to color stability and intensity. In material science, it is explored for its potential in creating advanced organic materials with specific optical or electronic characteristics.

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inventory 1g
10-20 days ฿30,240.00

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4,6-DIAMINO-2-METHYL-QUINOLINE
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Used primarily in the synthesis of pharmaceutical compounds, it serves as a key intermediate in the production of antimalarial drugs. Its structure is valuable in medicinal chemistry for developing molecules with potential therapeutic effects. Additionally, it is employed in research settings to study chemical reactions and mechanisms involving quinoline derivatives. Its applications extend to the development of dyes and pigments, where its chemical properties contribute to color stability and intensity.

Used primarily in the synthesis of pharmaceutical compounds, it serves as a key intermediate in the production of antimalarial drugs. Its structure is valuable in medicinal chemistry for developing molecules with potential therapeutic effects. Additionally, it is employed in research settings to study chemical reactions and mechanisms involving quinoline derivatives. Its applications extend to the development of dyes and pigments, where its chemical properties contribute to color stability and intensity. In material science, it is explored for its potential in creating advanced organic materials with specific optical or electronic characteristics.

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