37629-72-4

Basic information

• Product Name: (Z)-α-(3,4-dimethoxyphenyl)-3,4-dimethoxycinnamonitrile
• Synonyms: (Z)-α-(3,4-dimethoxyphenyl)-3,4-dimethoxycinnamonitrile
• CAS NO: 37629-72-4
• Molecular Weight: 325.364
• Mol File: 37629-72-4.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: (Z)-α-(3,4-dimethoxyphenyl)-3,4-dimethoxycinnamonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: (Z)-α-(3,4-dimethoxyphenyl)-3,4-dimethoxycinnamonitrile(37629-72-4)
• EPA Substance Registry System: (Z)-α-(3,4-dimethoxyphenyl)-3,4-dimethoxycinnamonitrile(37629-72-4)

Safety Data

• Hazardous Substances Data: 37629-72-4(Hazardous Substances Data)

Upstream product

• 93-17-4 3,4-dimethoxyphenylacetonitrile 
• 2460-33-5 3,4-dimethoxyphenylpyruvic acid 
• 120-14-9 3,4-dimethoxy-benzaldehyde 

Downstream Products

• 1346463-32-8 (E)-2,3-bis(3,4-dimethoxyphenyl)acrylaldehyde 
• 1359741-15-3 (3,4-bis(3,4-dimethoxyphenyl)-1H-pyrrol-2-yl)methanol 
• 1359741-12-0 ethyl 3,4-bis(3,4-dimethoxyphenyl)-1H-pyrrole-2-carboxylate 
• 1346463-58-8 4,5-bis(3,4-dimethoxyphenyl)penta-(2E,4Z)-dienoyl azide 
• 1346463-45-3 4,5-bis(3,4-dimethoxyphenyl)penta-(2E,4Z)-dienoic acid 
• 67189-18-8 (E)-α-(3,4-dimethoxyphenyl)-3,4-dimethoxycinnamonitrile 
• 1150647-77-0 10-cyano-2,3,5,6-tetramethoxyphenanthrene 
• 87226-94-6 2,3,6,7-tetramethoxyphenanthrene-9-carbonitrile 

Relevant articles and documents

PHENANTHROINDOLIZIDINE AND PHENANTHROQUINOLIZIDINE ALKALOID HAVING A HYDROXYL GROUP ON THE PHENANTHRENE RING THEREOF, PREPARATION METHOD AND USE THEREOF

A phenanthroindolizidine and phenanthroquinolizidine alkaloid having a hydroxyl group on the phenanthrene ring thereof was synthesized, which exhibits potent activity as an anticancer agent against, such as breast cancer, lung cancer, and prostate cancer.

Oxidative intramolecular coupling of 2,3-disubstituted phenyl acrylic acids and derivatives promoted by di-tert-butylperoxide

Polymethoxy-substituted phenanthrene-9-carboxylic acids or their methylate are key intermediates for the synthesis of tylophora alkaloids and their analogs. An intramolecular oxidative coupling reaction of unfunctionalized 2,3-disubstituted phenyl acrylic

Peripherally fused porphyrins via the Scholl reaction: Synthesis, self-assembly, and mesomorphism

Oxidative coupling of activated aryl groups attached to β-positions of the porphyrin ring provides convenient access to derivatives containing peripherally fused phenanthrene and benzo[g]chrysene units. Tetra(benzochryseno) porphyrin, reported here for the first time, contains a nonplanar, sterically locked π system and shows very intense electronic absorptions in the Q range of the electronic spectrum. Tetraphenanthroporphyrins show a tendency to aggregate in solution. In one case, a discrete dimer is formed, whose structure was investigated spectroscopically and theoretically. Derivatives bearing long alkyl chains are mesomorphic and exhibit columnar phases (tetraphenanthroporphyrins) and a monoclinic 3D phase (tetrabenzochrysenoporphyrin). The symmetry of column packing in the columnar phases is dependent on the number of alkyl chains per molecule. X-ray diffraction measurements show that, in spite of their nonplanarity, the aromatic cores in the mesophases are tightly stacked within the column. The corresponding stacking patterns were derived from the structure of the dimer, on the basis of geometrical analysis and molecular modeling.