4-Chloro-7-methoxy-2,3-dimethylquinoline

95%

Reagent Code: #46687
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CAS Number 1207-67-6

science Other reagents with same CAS 1207-67-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 221.68 g/mol
Formula C₁₂H₁₂ClNO
badge Registry Numbers
MDL Number MFCD26526905
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

Used primarily in pharmaceutical research, this compound serves as a key intermediate in the synthesis of various bioactive molecules. Its quinoline core structure makes it valuable in the development of potential drugs targeting infectious diseases, particularly antimalarial and antimicrobial agents. Additionally, it is employed in organic synthesis to create complex heterocyclic compounds, which are often explored for their therapeutic properties. Its specific substitution pattern enhances its reactivity and selectivity in chemical reactions, making it a useful building block in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿31,410.00

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4-Chloro-7-methoxy-2,3-dimethylquinoline
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Used primarily in pharmaceutical research, this compound serves as a key intermediate in the synthesis of various bioactive molecules. Its quinoline core structure makes it valuable in the development of potential drugs targeting infectious diseases, particularly antimalarial and antimicrobial agents. Additionally, it is employed in organic synthesis to create complex heterocyclic compounds, which are often explored for their therapeutic properties. Its specific substitution pattern enhances its reactivi

Used primarily in pharmaceutical research, this compound serves as a key intermediate in the synthesis of various bioactive molecules. Its quinoline core structure makes it valuable in the development of potential drugs targeting infectious diseases, particularly antimalarial and antimicrobial agents. Additionally, it is employed in organic synthesis to create complex heterocyclic compounds, which are often explored for their therapeutic properties. Its specific substitution pattern enhances its reactivity and selectivity in chemical reactions, making it a useful building block in medicinal chemistry.

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