1286282-28-7

Upstream product

• 112934-63-1 1-(4Methoxyphenyl)-1H-indole-2,3-dione 
• 91-56-5 indole-2,3-dione 
• 34137-14-9 methyl 4-hydroxy-3,5-dimethylbenzoate 
• 4919-37-3 3,5-dimethyl-4-hydroxybenzoic acid 
• 1307863-96-2 C₂₄H₁₉NO₅ 
• 1373514-02-3 C₂₅H₂₁NO₅ 
• 42293-38-9 C₉H₉ClO₂ 
• 130266-57-8 2-methoxyacridine-9-carboxylic acid 
• 104-92-7 1-bromo-4-methoxy-benzene 

Downstream Products

• 1392236-23-5 C₂HF₃O₂*C₃₉H₅₂N₄O₁₀S₂ 
• 1373514-09-0 C₄₈H₆₁N₅O₁₅S₂ 
• 1373514-04-5 C₂₉H₂₉NO₈S 
• 1420991-62-3 C₅₅H₇₈N₇O₁₇S₃⁽¹⁺⁾ 
• 1420991-61-2 C₄₆H₆₉N₆O₁₂S₃⁽¹⁺⁾ 
• 1420991-60-1 C₃₆H₄₆N₃O₁₀S₂⁽¹⁺⁾ 
• 1420991-59-8 C₃₇H₄₈N₃O₁₀S₂⁽¹⁺⁾ 
• 1420991-66-7 C₃₆H₃₄F₂NO₈S⁽¹⁺⁾ 

Relevant academic research and scientific papers

N-ALKYLATION OF ACRIDANS

The present invention provides compounds used in the synthesis of chemiluminescent acridinium compounds and methods of producing these compounds. Specifically, methods are provided for the N-alkylation of acridan compounds using alkylating reagents. Typically, these alkylating reagents comprise a protected sulfonate group protected with an acid-labile protecting group.

Chemiluminescence from alkoxy-substituted acridinium dimethylphenyl ester labels

Chemiluminescent acridinium dimethylphenyl ester labels are used in automated immunoassays for clinical diagnostics. Light emission from these labels is triggered by alkaline peroxide in the presence of the cationic surfactant cetyltrimethylammonium chlor