4-Chloro-6,7-dimethoxyquinoline-3-carbonitrile

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Reagent Code: #162980
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CAS Number 214470-55-0

science Other reagents with same CAS 214470-55-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 248.67 g/mol
Formula C₁₂H₉ClN₂O₂
badge Registry Numbers
MDL Number MFCD09261351
thermostat Physical Properties
Boiling Point 404.2 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, inert gas storage

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports the creation of compounds with high selectivity toward specific signaling pathways involved in tumor growth. Also utilized in research for designing novel antimicrobial and anti-inflammatory agents due to its electron-deficient aromatic core and functional group compatibility. Commonly employed in cross-coupling reactions to build complex quinoline-based molecules in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿7,920.00
inventory 1g
10-20 days ฿19,800.00
inventory 5g
10-20 days ฿59,340.00

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4-Chloro-6,7-dimethoxyquinoline-3-carbonitrile
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports the creation of compounds with high selectivity toward specific signaling pathways involved in tumor growth. Also utilized in research for designing novel antimicrobial and anti-inflammatory agents due to its electron-deficient aromatic core and functional group compatibility. Commonly employed in cross-coupling reactions to build complex

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports the creation of compounds with high selectivity toward specific signaling pathways involved in tumor growth. Also utilized in research for designing novel antimicrobial and anti-inflammatory agents due to its electron-deficient aromatic core and functional group compatibility. Commonly employed in cross-coupling reactions to build complex quinoline-based molecules in medicinal chemistry.

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