829-48-1

Basic information

• Product Name: ethyl 4-methoxybenzenecarboximidoate
• Synonyms: Ethyl 4-methoxyphenylimidoformate
• CAS NO: 829-48-1
• Molecular Formula: C₁₀H₁₃NO₂
• Molecular Weight: 179.2157
• Mol File: 829-48-1.mol
• Article Data: 16

Chemical Properties

• Boiling Point: 238.847°C at 760 mmHg
• Flash Point: 98.252°C
• Density: 1.036g/cm³
• Vapor Pressure: 0.064mmHg at 25°C
• Refractive Index: 1.494
• CAS DataBase Reference: ethyl 4-methoxybenzenecarboximidoate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 4-methoxybenzenecarboximidoate(829-48-1)
• EPA Substance Registry System: ethyl 4-methoxybenzenecarboximidoate(829-48-1)

Safety Data

• Hazardous Substances Data: 829-48-1(Hazardous Substances Data)

Upstream product

• 64-17-5 ethanol 
• 874-90-8 4-methoxybenzonitrile 
• 75-03-6 ethyl iodide 
• 75-36-5 acetyl chloride 

Downstream Products

• 6926-51-8 5-(4-methoxyphenyl)-1H-tetrazole 
• 138190-42-8 2-(4-methoxy-phenyl)-5-(1-methyl-butylidene)-3,5-dihydro-imidazol-4-one 
• 72684-11-8 N'-Phenyl-<4-methoxy-benzamidrazon> 
• 1622-11-3 3-(4-methoxyphenyl)-1,5-diphenylformazan 
• 138190-43-9 5-(4-methoxy-cyclohexyLiDene)-2-(4-methoxy-phenyl)-3,5-dihydro-imidazol-4-one 
• 2564-57-0 4-carbomethoxy-2-(4-methoxyphenyl)-δ²-thiazoline 
• 10602-66-1 O-ethyl 4-methoxythiobenzoate 
• 92666-91-6 2-[6,7-Dimethoxy-2-(4-methoxy-benzoyl)-1,2,3,4-tetrahydro-isoquinolin-1-yl]-acetamide 
• 159053-06-2 5-(4-methoxylphenyl)-3-(2-pyrazinyl)-1H-1,2,4-triazole 
• 935750-39-3 1,2-bis(4-methoxyphenyl)-2-imidazoline 
• 852525-37-2 1,2-bis(4-methoxyphenyl)-1H-imidazole 
• 84951-40-6 2-(4-methoxyphenyl)-4H-thiopyrano[2,3-b]pyridin-4-one 
• 125554-45-2 p-methoxyphenyl-2 (4H) pyrido <3,2-e>-thiazine-1,3 one-4 
• 125536-17-6 p-methoxyphenyl-2 dihydro-2,3 (4H) pyrido <3,2-e>-thiazine-1,3 one-4 

Relevant articles and documents

Synthesis of Highly Fused Pyrano[2,3- b]pyridines via Rh(III)-Catalyzed C-H Activation and Intramolecular Cascade Annulation under Room Temperature

A facile access to the polycyclic-fused pyrano[2,3-b]pyridines has been established under room temperature via Rh(III)-catalyzed C-H bond activation and intramolecular cascade annulation. This strategy features high efficiency, unique versatility, and gen

An efficient, stereocontrolled and versatile synthetic route to bicyclic partially saturated privileged scaffolds

Herein, we describe the development of a simple, high yielding and stereocontrolled strategy for the synthesis of a series of triazolopiperazines and other biologically relevant fused scaffolds from optically active amino acids. This route was applied to the synthesis of 22 scaffolds containing new, previously inaccessible vectors and used to access a novel analogue of ganaplacide.

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