2-CHLORO-N-(6-METHOXY-4-QUINOLINYL)-5-NITRO-BENZAMIDE

98%

Reagent Code: #163746
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CAS Number 2088135-12-8

science Other reagents with same CAS 2088135-12-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 357.75 g/mol
Formula C₁₇H₁₂ClN₃O₄
badge Registry Numbers
MDL Number MFCD31656711
thermostat Physical Properties
Boiling Point 492.3±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.469±0.06 g/cm3(Predicted)
Storage Room temperature, light-proof, inert gas

description Product Description

Used as an intermediate in the synthesis of quinoline-based pharmaceutical compounds, particularly in the development of antimalarial and antimicrobial agents. Its structure supports binding to biological targets involved in pathogen replication, making it valuable in medicinal chemistry research. Also employed in the preparation of kinase inhibitors for potential use in cancer therapy. Commonly utilized in laboratory settings for structure-activity relationship (SAR) studies due to its electron-withdrawing and hydrogen-bonding features.

Available Sizes & Pricing

Size Availability Unit Price Quantity
25mg
10-20 days ฿10,430.00
50mg
10-20 days ฿16,220.00
100mg
10-20 days ฿26,690.00
250mg
10-20 days ฿47,750.00
2-CHLORO-N-(6-METHOXY-4-QUINOLINYL)-5-NITRO-BENZAMIDE
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Used as an intermediate in the synthesis of quinoline-based pharmaceutical compounds, particularly in the development of antimalarial and antimicrobial agents. Its structure supports binding to biological targets involved in pathogen replication, making it valuable in medicinal chemistry research. Also employed in the preparation of kinase inhibitors for potential use in cancer therapy. Commonly utilized in laboratory settings for structure-activity relationship (SAR) studies due to its electron-withdraw

Used as an intermediate in the synthesis of quinoline-based pharmaceutical compounds, particularly in the development of antimalarial and antimicrobial agents. Its structure supports binding to biological targets involved in pathogen replication, making it valuable in medicinal chemistry research. Also employed in the preparation of kinase inhibitors for potential use in cancer therapy. Commonly utilized in laboratory settings for structure-activity relationship (SAR) studies due to its electron-withdrawing and hydrogen-bonding features.

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