2-Chloro-6-methylquinoline-3-carbonitrile

≥95%

Reagent Code: #129198
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CAS Number 483287-37-2

science Other reagents with same CAS 483287-37-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 202.64 g/mol
Formula C₁₁H₇ClN₂
badge Registry Numbers
MDL Number MFCD03045343
thermostat Physical Properties
Melting Point 177-178 °C
Boiling Point 373.4 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.31 g/cm3
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of quinoline-based pharmaceuticals, particularly in antimalarial and anticancer agents. Its nitrile and chloro functional groups allow for selective modifications, enabling the development of targeted drug candidates. Also employed in agrochemical research for designing novel pesticides with improved efficacy and selectivity. The compound's aromatic structure supports conjugation in organic electronic materials, explored in some specialty applications.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿6,600.00
inventory 1g
10-20 days ฿18,700.00

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2-Chloro-6-methylquinoline-3-carbonitrile
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Used as a key intermediate in the synthesis of quinoline-based pharmaceuticals, particularly in antimalarial and anticancer agents. Its nitrile and chloro functional groups allow for selective modifications, enabling the development of targeted drug candidates. Also employed in agrochemical research for designing novel pesticides with improved efficacy and selectivity. The compound's aromatic structure supports conjugation in organic electronic materials, explored in some specialty applications.

Used as a key intermediate in the synthesis of quinoline-based pharmaceuticals, particularly in antimalarial and anticancer agents. Its nitrile and chloro functional groups allow for selective modifications, enabling the development of targeted drug candidates. Also employed in agrochemical research for designing novel pesticides with improved efficacy and selectivity. The compound's aromatic structure supports conjugation in organic electronic materials, explored in some specialty applications.

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