2-Chloro-6-methoxy-4-methylquinoline

95%

Reagent Code: #163249
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CAS Number 6340-55-2

science Other reagents with same CAS 6340-55-2

blur_circular Chemical Specifications

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Weight 207.66 g/mol
Formula C₁₁H₁₀ClNO
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MDL Number MFCD00087558
inventory_2 Storage & Handling
Density 1.287 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antimalarial and anticancer agents. Its structure supports the creation of complex quinoline-based compounds that exhibit biological activity. Also employed in research for developing new organic materials and catalysts due to its electron-rich aromatic system. Shows potential in agrochemical applications as a building block for herbicides and pesticides. Its chloro and methoxy functional groups allow for selective modifications, making it valuable in medicinal chemistry for structure-activity relationship studies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,800.00
inventory 250mg
10-20 days ฿4,680.00
inventory 1g
10-20 days ฿13,730.00

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2-Chloro-6-methoxy-4-methylquinoline
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antimalarial and anticancer agents. Its structure supports the creation of complex quinoline-based compounds that exhibit biological activity. Also employed in research for developing new organic materials and catalysts due to its electron-rich aromatic system. Shows potential in agrochemical applications as a building block for herbicides and pesticides. Its chloro and methoxy functional groups allow for sele

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antimalarial and anticancer agents. Its structure supports the creation of complex quinoline-based compounds that exhibit biological activity. Also employed in research for developing new organic materials and catalysts due to its electron-rich aromatic system. Shows potential in agrochemical applications as a building block for herbicides and pesticides. Its chloro and methoxy functional groups allow for selective modifications, making it valuable in medicinal chemistry for structure-activity relationship studies.

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