2-Chloro-7-methylquinoline-3-carbonitrile

95%

Reagent Code: #163566
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CAS Number 79249-34-6

science Other reagents with same CAS 79249-34-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 202.64 g/mol
Formula C₁₁H₇ClN₂
badge Registry Numbers
MDL Number MFCD08437564
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antimalarial and anticancer agents. Its structure supports the formation of quinoline-based bioactive molecules, which are known for their interaction with biological targets such as enzymes and receptors. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies to enhance drug potency and selectivity. Also utilized in the preparation of fluorescent probes due to the inherent photophysical properties of the quinoline scaffold.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,000.00
inventory 500mg
10-20 days ฿9,600.00
inventory 1g
10-20 days ฿12,800.00
inventory 5g
10-20 days ฿38,400.00
inventory 250mg
10-20 days ฿6,400.00
inventory 10g
10-20 days ฿64,000.00

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2-Chloro-7-methylquinoline-3-carbonitrile
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antimalarial and anticancer agents. Its structure supports the formation of quinoline-based bioactive molecules, which are known for their interaction with biological targets such as enzymes and receptors. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies to enhance drug potency and selectivity. Also utilized in the preparation of fluorescent probes due to the

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antimalarial and anticancer agents. Its structure supports the formation of quinoline-based bioactive molecules, which are known for their interaction with biological targets such as enzymes and receptors. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies to enhance drug potency and selectivity. Also utilized in the preparation of fluorescent probes due to the inherent photophysical properties of the quinoline scaffold.

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