18101-88-7

Upstream product

• 64-17-5 ethanol 
• 25117-74-2 4-ethoxybenzonitrile 
• 767-00-0 4-cyanophenol 

Downstream Products

• 59855-69-5 chlorure d'ethoxy-4 benzamidinium 
• 1441097-23-9 3,6-diethoxy-1-tosyl-1H-indazole 
• 13451-87-1 4-ethoxy-thiobenzoic acid O-(2-diethylamino-ethyl ester) 
• 13451-88-2 4-ethoxy-thiobenzoic acid S-(2-diethylamino-ethyl ester) 
• 94-23-5 parethoxycaine 
• 125575-08-8 C₂₃H₁₆O₆*C₁₅H₂₅N₃O 
• 125575-09-9 methanesulfonate de N-<<(methylenedioxy-3,4 benzyl)-4 piperazinyl>-2 ethyl> ethoxy-4 benzamidinium 
• 125575-10-2 N-[2-(4-Benzo[1,3]dioxol-5-ylmethyl-piperazin-1-yl)-ethyl]-4-ethoxy-benzamidine; hydrochloride 
• 135420-42-7 N-(2-Diethylamino-ethyl)-4-ethoxy-benzamidine; hydrochloride 
• 15504-06-0 4-ethoxy-thiobenzoic acid O-ethyl ester 

Relevant academic research and scientific papers

Rhodium-Catalyzed Relay Carbenoid Functionalization of Aromatic C-H Bonds toward Fused Heteroarenes

A rhodium-catalyzed annulation between ethyl benzimidates and α- aroyl sulfur ylides was developed, affording a series of pyrano[4,3,2-ij]isoquinoline derivatives in moderate to good yields with good functional group compatibility. The procedure featured

Synthesis of 1H-Indazoles from Imidates and Nitrosobenzenes via Synergistic Rhodium/Copper Catalysis

Nitrosobenzenes have been used as a convenient aminating reagent for the efficient synthesis of 1H-indazoles via rhodium and copper catalyzed C-H activation and C-N/N-N coupling. The reaction occurred under redox-neutral conditions with high efficiency and functional group tolerance. Moreover, a rhodacyclic imidate complex has been identified as a key intermediate.

Rh(III)-Catalyzed C-C/C-N Coupling of Imidates with α-Diazo Imidamide: Synthesis of Isoquinoline-Fused Indoles

Imidate esters and diazo compounds have been established as bifunctional substrates for the construction of biologically active fused heterocycles via rhodium-catalyzed C-H activation and C-C/C-N coupling. This reaction occurs under mild conditions with high efficiency, step economy, and low catalyst loading.

Anti-arythmiques apparentes au procainamide II. Synthese et etude pharmacologique

Anti-arrhythmic agents related to procainamide II.Synthesis and pharmacological study.In view of their marked anti-arrhythmic activity, we continued our studies on the N--4-alkoxy-benzamidines described previously.We prepared p