2,4-Dichloro-3,6-dimethylquinoline

98%

Reagent Code: #177552
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CAS Number 1936054-65-7

science Other reagents with same CAS 1936054-65-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 226.10 g/mol
Formula C₁₁H₉Cl₂N
inventory_2 Storage & Handling
Storage Room temperature, light-proof storage, dry seal

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure supports the development of compounds with biological activity, particularly in herbicides and antimicrobial agents. Commonly employed in research settings for the preparation of quinoline-based derivatives that exhibit potential therapeutic properties. Also utilized in the manufacturing of dyes and pigments due to its aromatic and electron-rich framework. Its chlorinated and methylated features enhance reactivity in coupling reactions, making it valuable in organic synthesis and medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿13,260.00
inventory 250mg
10-20 days ฿22,140.00

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2,4-Dichloro-3,6-dimethylquinoline
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure supports the development of compounds with biological activity, particularly in herbicides and antimicrobial agents. Commonly employed in research settings for the preparation of quinoline-based derivatives that exhibit potential therapeutic properties. Also utilized in the manufacturing of dyes and pigments due to its aromatic and electron-rich framework. Its chlorinated and methylated features enhance reactivit

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure supports the development of compounds with biological activity, particularly in herbicides and antimicrobial agents. Commonly employed in research settings for the preparation of quinoline-based derivatives that exhibit potential therapeutic properties. Also utilized in the manufacturing of dyes and pigments due to its aromatic and electron-rich framework. Its chlorinated and methylated features enhance reactivity in coupling reactions, making it valuable in organic synthesis and medicinal chemistry.

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