1151666-74-8

Basic information

• Product Name: (Z)-3-(2,3,4-trimethoxyphenyl)-2-(3,4-dimethoxyphenyl)acrylonitrile
• Synonyms: (Z)-3-(2,3,4-trimethoxyphenyl)-2-(3,4-dimethoxyphenyl)acrylonitrile
• CAS NO: 1151666-74-8
• Molecular Weight: 355.39
• Mol File: 1151666-74-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (Z)-3-(2,3,4-trimethoxyphenyl)-2-(3,4-dimethoxyphenyl)acrylonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: (Z)-3-(2,3,4-trimethoxyphenyl)-2-(3,4-dimethoxyphenyl)acrylonitrile(1151666-74-8)
• EPA Substance Registry System: (Z)-3-(2,3,4-trimethoxyphenyl)-2-(3,4-dimethoxyphenyl)acrylonitrile(1151666-74-8)

Safety Data

• Hazardous Substances Data: 1151666-74-8(Hazardous Substances Data)

Upstream product

• 93-17-4 3,4-dimethoxyphenylacetonitrile 
• 2103-57-3 2,3,4-trimethoxybenzaldehyde 

Relevant articles and documents

Cyano Group Removal from Cyano-Promoted Aza-Diels-Alder Adducts: Synthesis and Structure-Activity Relationship of Phenanthroindolizidines and Phenanthroquinolizidines

Phenanthroindolizidines and phenanthroquinolizidines were concisely synthesized by the reductive decyanization of cyano-promoted intramolecular aza-Diels-Alder cycloadducts followed by aryl-aryl coupling. Cyano groups were removed from α-aminoacrylonitriles via treatment with sodium borohydride in 2-propanol in almost quantitative yields; a possible mechanism was proposed and examined using D-labeling experiments. A systematic study of the effects of the phenanthrene substitution pattern on the anticancer activity against three human cancer cell lines was discussed. (Chemical Equation Presented).

Process of preparing discotic liquid crystalline compounds

The invention relates to a process of preparing a discotic liquid crystalline compound by intramolecular oxidative cyclisation of a diaryl compound in an organic solvent in the presence of a strong acid, characterized in that an oxidative agent comprising a chrom(VI)oxide derivative is used, to discotic liquid crystalline compounds obtainable from said process, to liquid crystalline media, (co)polymers or polymer networks with columnar phases comprising said discotic liquid crystalline compounds, and to the use of said discotic liquid crystalline compounds, liquid crystalline media or liquid crystalline (co)polymers with columnar phases for liquid crystal displays, optical elements like polarizers, compensators or colour filters, chemical sensors, charge transport materials, optical storage media, nonlinear optics, decorative pigments, adhesive or synthetic resins with anisotropic mechanical properties.