35782-26-4

Basic information

• Product Name: 3-<(E)-2-Phenylethenyl>pyridazin
• Synonyms: 3-<(E)-2-Phenylethenyl>pyridazin
• CAS NO: 35782-26-4
• Molecular Weight: 182.225
• Mol File: 35782-26-4.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 3-<(E)-2-Phenylethenyl>pyridazin(CAS DataBase Reference)
• NIST Chemistry Reference: 3-<(E)-2-Phenylethenyl>pyridazin(35782-26-4)
• EPA Substance Registry System: 3-<(E)-2-Phenylethenyl>pyridazin(35782-26-4)

Safety Data

• Hazardous Substances Data: 35782-26-4(Hazardous Substances Data)

Upstream product

• 1632-76-4 3-methylpyridazine 
• 100-51-6 benzyl alcohol 
• 100-52-7 benzaldehyde 

Downstream Products

• 68031-27-6 3-(2-phenylethyl)pyridazine 
• 115984-36-6 (1α,2α,3β,4β)-1,3-Bis(3-pyridazinyl)-2,4-diphenylcyclobutan 
• 115984-35-5 (1α,2α,3β,4β)-1,2-Bis(3-pyridazinyl)-3,4-diphenylcyclobutan 

Relevant articles and documents

MnO2 mediated sequential oxidation/olefination of alkyl-substituted heteroarenes with alcohols

A practical and efficient ligand-free MnO2 mediated sequential oxidation and olefination has been developed for the facile synthesis of a broad range of unsaturated N-heteroazaarenes from simple alkyl-substituted heteroarenes and alcohols. The procedure tolerates a series of functional groups, such as methoxyl, chloro, bromo, iodo, vinyl, phenolic and hetero groups, providing the olefination products in moderate to good yields.The protocol could be conducted at mild conditions and used environmentally friendly air as the clear oxidant.

A trans-substituted olefin preparation method (by machine translation)

This invention relates to a trans-substituted olefin preparation method, which belongs to the technical field of organic chemical synthesis. The method adopts the simple alcohol and methyl nitrogen-containing heterocyclic as the starting material, by transition metal-catalyzed alkene base reaction, to obtain trans-substituted olefin compound. The reaction raw material, catalyst and additives is cheap, simple synthesis technology, greatly reduces the cost of synthesizing; mild reaction conditions, high yield, easy industrialization; the reaction of raw materials and catalyst cleaning toxic, small pollution to the environment. The trans-substituted olefin compound and its derivatives as an important fine chemicals, in the medical, agricultural chemicals, perfume and photoelectric and other industries have wide application. (by machine translation)

Photoreactions in Crystals with Ethenes: Selectivities and Crystal Engineering

Photoreactions in crystals of sterically hindered dimethylenecyclopentanones 1 and trimethylenecyclopentanes 4 lead to E/Z isomerizations and 1,5-H shifts.The stereochemical result of the photodimerization in the crystalline state of the heterostilbenes 6