6267-07-8

Basic information

• Product Name: (1E)-1,2-bis(3,4-dimethoxyphenyl)-N-hydroxyethanimine
• CAS NO: 6267-07-8
• Molecular Formula: C₁₈H₂₁NO₅
• Molecular Weight: 331.363
• Mol File: 6267-07-8.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 491.419°C at 760 mmHg
• Flash Point: 251.002°C
• Density: 1.143g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.527
• CAS DataBase Reference: (1E)-1,2-bis(3,4-dimethoxyphenyl)-N-hydroxyethanimine(CAS DataBase Reference)
• NIST Chemistry Reference: (1E)-1,2-bis(3,4-dimethoxyphenyl)-N-hydroxyethanimine(6267-07-8)
• EPA Substance Registry System: (1E)-1,2-bis(3,4-dimethoxyphenyl)-N-hydroxyethanimine(6267-07-8)

Safety Data

• Hazardous Substances Data: 6267-07-8(Hazardous Substances Data)

Usage

Description

(1E)-1,2-bis(3,4-dimethoxyphenyl)-N-hydroxyethanimine is a bisimine derivative with a molecular formula of C18H21NO3. It features a central N-hydroxyethanimine moiety flanked by two 3,4-dimethoxyphenyl groups. This chemical compound is recognized for its potential biological activities, such as antioxidant and antimicrobial properties, and may hold promise for applications in pharmaceutical research and drug development. However, further research is necessary to fully explore its properties and potential uses.

Uses

Used in Pharmaceutical Research:
(1E)-1,2-bis(3,4-dimethoxyphenyl)-N-hydroxyethanimine is used as a compound of interest in pharmaceutical research for its potential antioxidant and antimicrobial properties. These characteristics make it a candidate for the development of new drugs targeting various diseases and conditions.
Used in Drug Development:
In drug development, (1E)-1,2-bis(3,4-dimethoxyphenyl)-N-hydroxyethanimine may be utilized as a starting point for creating new pharmaceuticals. Its unique structure and potential biological activities could lead to the discovery of novel therapeutic agents.
Note: Since the provided materials do not specify different industries or detailed applications, the uses listed are general and based on the potential properties mentioned. Further research would be required to identify specific applications in various industries.

Upstream product

• 4927-55-3 1,2-bis(3,4-dimethoxyphenyl)ethanone 
• 5653-60-1 3,3',4,4'-tetramethoxybenzoin 
• 91-16-7 1,2-dimethoxybenzene 
• 554-34-7 1,2-bis(3,4-dimethoxyphenyl)ethane-1,2-dione 
• 10313-60-7 3,4-dimethoxyphenylacetyl chloride 
• 93-40-3 (3,4-Dimethoxyphenyl)acetic acid 

Downstream Products

• 5471-40-9 3,4,3',4'-tetramethoxy-bibenzyl-α-ylamine 
• 76306-62-2 N-<1,2-bis(3,4-dimethoxyphenyl)ethyl>acetamide 

Relevant articles and documents

Rh-catalyzed sequential oxidative C-H activation/annulation with geminal-substituted vinyl acetates to access isoquinolines

The concise synthesis of 3-substituted or non-C3-substituted isoquinolines through Rh-catalyzed sequential oxidative C-H activation/annulation with geminal-substituted vinyl acetates was developed with good functional group tolerance. The protocol was successfully applied to the total synthesis of the natural product papaverine.