233604-21-2

Basic information

• Product Name: 5-{4-[(E)-2-(4-Methylphenyl)ethen-1-yl]phenyl}tetrazole
• Synonyms: 5-{4-[(E)-2-(4-Methylphenyl)ethen-1-yl]phenyl}tetrazole
• CAS NO: 233604-21-2
• Molecular Weight: 262.314
• Mol File: 233604-21-2.mol

Chemical Properties

• CAS DataBase Reference: 5-{4-[(E)-2-(4-Methylphenyl)ethen-1-yl]phenyl}tetrazole(CAS DataBase Reference)
• NIST Chemistry Reference: 5-{4-[(E)-2-(4-Methylphenyl)ethen-1-yl]phenyl}tetrazole(233604-21-2)
• EPA Substance Registry System: 5-{4-[(E)-2-(4-Methylphenyl)ethen-1-yl]phenyl}tetrazole(233604-21-2)

Safety Data

• Hazardous Substances Data: 233604-21-2(Hazardous Substances Data)

Upstream product

• 41425-61-0 4-[(E)-2-(4-Methylphenyl)ethen-1-yl]benzonitrile 
• 1552-41-6 diethyl [(4-cyanophenyl)methyl]phosphonate 
• 104-87-0 4-methyl-benzaldehyde 

Relevant articles and documents

Solvent-dependent fluorescence of donor-substituted (E)-1,2-bis(stilbenyl-1,3,4-oxadiazolyl)ethenes

The Huisgen reaction of aryltetrazoles and fumaryl chloride leads to symmetrically aryl-substituted 1,2-bis(1,3,4-oxadiazolyl)ethenes. Molecules with extended conjugated systems are accessible using stilbenyltetrazoles or higher homologues. The substitution with solubility-permitting alkoxy side-chains results in molecules of C2h symmetry, consisting of a central electron-accepting segment and two terminal electron density-releasing units. The solvatochromism of the absorption spectra is negligible, while in the emission spectra a strong positive solvatochromism connected with a dramatic decrease of the quantum yield is observed, indicating intramolecular charge transfer. The influences of different alkoxy substitution patterns on the luminescence properties are discussed. Copyright

(E)-1,2-bis(5-aryl-1,3,4-oxadiazol-2-yl)ethenes

A series of (E)-1,2-bis(1,3,4-oxadiazol-2-yl)ethenes with a variety of aromatic substituents in the 5-positions of the heterocycles was prepared by acylation of the corresponding tetrazoles with fumaryl chloride and subsequent thermal ring transformation. The modified Huisgen reaction renders a new pathway to 3-(1,3,4-oxadiazol-2-yl)propenoic acids and subsequently to the title compounds with different substituents.