4-Chloroquinoline-6-carbonitrile

95%

Reagent Code: #81318
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CAS Number 219763-83-4

science Other reagents with same CAS 219763-83-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 188.61 g/mol
Formula C₁₀H₅ClN₂
badge Registry Numbers
MDL Number MFCD08063204
thermostat Physical Properties
Boiling Point 340.3°C at 760 mmHg
inventory_2 Storage & Handling
Storage -20°C, dry sealed

description Product Description

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical agents. It serves as a building block for the development of quinoline-based drugs, which are known for their diverse biological activities. Specifically, it is employed in the creation of compounds with potential anti-malarial, anti-cancer, and anti-inflammatory properties. Researchers also explore its use in designing molecules that target specific enzymes or receptors, contributing to the advancement of targeted therapies. Additionally, its structural features make it valuable in the study of structure-activity relationships (SAR) to optimize drug efficacy and safety.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿10,170.00
inventory 100mg
10-20 days ฿5,157.00
inventory 1g
10-20 days ฿25,425.00

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4-Chloroquinoline-6-carbonitrile
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This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical agents. It serves as a building block for the development of quinoline-based drugs, which are known for their diverse biological activities. Specifically, it is employed in the creation of compounds with potential anti-malarial, anti-cancer, and anti-inflammatory properties. Researchers also explore its use in designing molecules that target specific enzymes or receptor

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical agents. It serves as a building block for the development of quinoline-based drugs, which are known for their diverse biological activities. Specifically, it is employed in the creation of compounds with potential anti-malarial, anti-cancer, and anti-inflammatory properties. Researchers also explore its use in designing molecules that target specific enzymes or receptors, contributing to the advancement of targeted therapies. Additionally, its structural features make it valuable in the study of structure-activity relationships (SAR) to optimize drug efficacy and safety.

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