93270-42-9

Basic information

• Product Name: ethyl (1Z)-2-(3,4,5-trimethoxyphenyl)ethanimidoate
• CAS NO: 93270-42-9
• Molecular Formula: C₁₃H₁₉NO₄*ClH
• Molecular Weight: 253.2943
• Mol File: 93270-42-9.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 335.3°C at 760 mmHg
• Flash Point: 156.6°C
• Density: 1.08g/cm³
• Vapor Pressure: 0.000235mmHg at 25°C
• Refractive Index: 1.484
• CAS DataBase Reference: ethyl (1Z)-2-(3,4,5-trimethoxyphenyl)ethanimidoate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl (1Z)-2-(3,4,5-trimethoxyphenyl)ethanimidoate(93270-42-9)
• EPA Substance Registry System: ethyl (1Z)-2-(3,4,5-trimethoxyphenyl)ethanimidoate(93270-42-9)

Safety Data

• Hazardous Substances Data: 93270-42-9(Hazardous Substances Data)

Upstream product

• 64-17-5 ethanol 
• 13338-63-1 2-(3,4,5-trimethoxyphenyl)acetonitrile 

Downstream Products

• 101-30-4 2-(3,4,5-trimethoxy-benzyl)-4,5-dihydro-1H-imidazole 
• 137206-50-9 3,4,5-trimethoxyphenylmethyl-β-3,4,5-trimethoxyphenylacetylamidrazone 
• 141245-91-2 3-[2-(3,4,5-Trimethoxy-benzyl)-benzoimidazol-1-yl]-butyric acid 
• 93270-44-1 N-(2,2-Dimethoxy-ethyl)-2-(3,4,5-trimethoxy-phenyl)-acetamidine; hydrochloride 
• 137206-47-4 3-(3,4,5-trimethoxyphenylmethyl)-5-(3,4,5-trimethoxyphenyl)-1,2,4-triazole 
• 137206-46-3 bis-3,5-(3,4,5-trimethoxyphenylmethyl)-1,2,4-triazole 
• 1041643-93-9 C₁₄H₁₈N₂O₅ 

Relevant articles and documents

Rapid synthesis and lipase inhibition activity of some new benzimidazole and perimidine derivatives

This study presents a synthesis of new series of some benzimidazole, bisbenzimidazole and perimidine derivatives via microwave technique, which, leads to the good product yields and short reaction times. The structure of newly synthesized compounds was confirmed by 1H NMR and 13C NMR spectra. These compounds were screened for their lipase inhibition activity. Then, all compounds were evaluated with regard to pancreatic lipase activity, and some of the 2-substituted perimidines, bisperimidine and bisbenzimidazole derivatives showed lipase inhibition at various concentrations.

Synthesis and choleretic activity of 3-[2-(3-R', 4-R'', 5-R'''-benzyl)-5- R-benzimidazol-1-yl]-butanoic acids

On the ground of the evidentiated choleretic activity of 3-[2- benzylbenzimidazol-1-yl]butanoic acid, 28 new acids were prepared in order to evaluate the influence of suitable substitutions in either C5 of heteroring or C3', C4', C5' of benzyl group in po

Synthesis and reactions of 2-amino-7,8-dimethoxy-1H-3-benzazepines. Competitive formation of 2-amino-1H-3-benzazepines VS. 2-benzylimidazoles

A short synthesis of 2-amino-7,8-dimethoxy-1H-3-benzazepine (1a) from 3,4-dimethoxyphenylacetonitrile is reported. The synthesis of several other 2-amino-1H-3-benzazepines 1 is also discussed. Conditions which favor the formation of 1 versus the formation