50593-65-2

Usage

Uses

Used in Pharmaceutical Industry:
Used in Chemical Synthesis:
In the chemical industry, 8-chloro-6-methyl[1,3]dioxolo[4,5-g]quinoline(SALTDATA: FREE) serves as an intermediate or building block for the synthesis of more complex molecules with potential applications in various fields, such as materials science, agrochemicals, and pharmaceuticals. Its unique structure allows for further functionalization and modification to create novel compounds with desired properties.

InChI:InChI=1/C11H8ClNO2/c1-6-2-8(12)7-3-10-11(15-5-14-10)4-9(7)13-6/h2-4H,5H2,1H3

Upstream product

• 50593-64-1 6-metil-8-ossi-1,3-diossol<4,5-g>chinolina 
• 91918-88-6 β-(3,4-metilendiossifenilammino)crotonato di etile 
• 14268-66-7 benzo[1,3]dioxolo-5-ylamine 

Downstream Products

• 91918-90-0 6-metil-8-idrazino-1,3-diossol<4,5-g>chinolina 
• 91918-89-7 6-metil-8-mercapto-1,3-diossol<4,5-g>chinolina 
• 91918-93-3 N-[1-(4-Chloro-phenyl)-meth-(E)-ylidene]-N'-(6-methyl-[1,3]dioxolo[4,5-g]quinolin-8-yl)-hydrazine 
• 91918-95-5 N-[1-(4-Bromo-phenyl)-meth-(E)-ylidene]-N'-(6-methyl-[1,3]dioxolo[4,5-g]quinolin-8-yl)-hydrazine 
• 91918-94-4 N-[1-(4-Fluoro-phenyl)-meth-(E)-ylidene]-N'-(6-methyl-[1,3]dioxolo[4,5-g]quinolin-8-yl)-hydrazine 
• 91918-97-7 NSC₃₃₂₃₈₄ 
• 91919-02-7 NSC332389 
• 91918-96-6 N-(6-Methyl-[1,3]dioxolo[4,5-g]quinolin-8-yl)-N'-[1-(4-nitro-phenyl)-meth-(E)-ylidene]-hydrazine 
• 91919-09-4 NSC332397 
• 91919-01-6 N-(6-Methyl-[1,3]dioxolo[4,5-g]quinolin-8-yl)-N'-[1-(2,4,6-trimethoxy-phenyl)-meth-(E)-ylidene]-hydrazine 
• 1038623-55-0 6-methyl-8-(4-nitrophenoxy)[1,3]dioxolo[4,5-g]quinoline 

Relevant academic research and scientific papers

Potent DNA-directed alkylating agents: Synthesis and biological activity of phenyl N-mustard-quinoline conjugates having a urea or hydrazinecarboxamide linker

A series of N-mustard-quinoline conjugates bearing a urea or hydrazinecarboxamide linker was synthesized for antitumor evaluation. The in vitro cytotoxicity studies revealed that compounds with hydrazinecarboxamide linkers were generally more cytotoxic th

SINTESI ED ATTIVITA BIOLOGICA DI NUOVI COMPOSTI A STRUTTURA 1,3-DIOSSOL CHINOLINICA

The synthesis of some 1,3-dioxol quinoline derivatives is described.The compounds show appreciable activity in vitro against P388 lymphocytic leukemia.Microbiological and antitumor results are presented.