18101-88-7

Basic information

• Product Name: ethoxy-4 benzimidate d'ethyle
• Synonyms: ethoxy-4 benzimidate d'ethyle
• CAS NO: 18101-88-7
• Molecular Weight: 193.246
• Mol File: 18101-88-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: ethoxy-4 benzimidate d'ethyle(CAS DataBase Reference)
• NIST Chemistry Reference: ethoxy-4 benzimidate d'ethyle(18101-88-7)
• EPA Substance Registry System: ethoxy-4 benzimidate d'ethyle(18101-88-7)

Safety Data

• Hazardous Substances Data: 18101-88-7(Hazardous Substances Data)

Upstream product

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

Downstream Products

• 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 
• 59855-69-5 chlorure d'ethoxy-4 benzamidinium 
• 15504-06-0 4-ethoxy-thiobenzoic acid O-ethyl ester 

Relevant articles and documents

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

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.