125311-40-2

Basic information

• Product Name: Pyridine, 2,6-bis[(1E)-2-phenylethenyl]-
• CAS NO: 125311-40-2
• Molecular Formula: C21H17N
• Molecular Weight: 283.373
• Mol File: 125311-40-2.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Pyridine, 2,6-bis[(1E)-2-phenylethenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Pyridine, 2,6-bis[(1E)-2-phenylethenyl]-(125311-40-2)
• EPA Substance Registry System: Pyridine, 2,6-bis[(1E)-2-phenylethenyl]-(125311-40-2)

Safety Data

• Hazardous Substances Data: 125311-40-2(Hazardous Substances Data)

Upstream product

• 108-48-5 2,6-dimethylpyridine 
• 100-52-7 benzaldehyde 
• 100-46-9 benzylamine 
• 7703-74-4 2,6-bis-(bromomethyl)pyridine 
• 123705-92-0 2,6-bis[benzylsulfanylmethyl]pyridine 
• 1410785-96-4 2,6-bis[benzylsulfonylmethyl]pyridine 
• 780-21-2 N-(4-chlorobenzylidene)aniline 

Downstream Products

• 818377-18-3 Norlobelane 
• 125311-41-3 (E,E)-2,6-bis(2-phenylethenyl)pyridine-1-oxide 
• 116539-72-1 2,6-bis-(4-nitro-trans-styryl)-pyridine 
• 68031-94-7 2,6-bis (2-phenylethyl) pyridine 
• 5302-71-6 1-methyl-2,6-di-trans-styryl-pyridinium; iodide 

Relevant articles and documents

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Deaminative Olefination of Methyl N-Heteroarenes by an Amine Oxidase Inspired Catalyst

We explored the bioinspired o-quinone cofactor catalyzed aerobic primary amine dehydrogenation for a cascade olefination reaction with nine different methyl N-heteroarenes, including pyrimidines, pyrazines, pyridines, quinolines, quinoxolines, benzimidazoles, benzoxazoles, benzthiazoles, and triazines. An o-quinone catalyst phd (1,10-phenanthroline-5,6-dione) combined with a Br?nsted acid catalyzed the reaction. N-Heteroaryl stilbenoids were synthesized in high yields and (E)-selectivities under mild conditions using oxygen (1 atm) as the sole oxidant without needing transition-metal salt, ligand, stoichiometric base, or oxidant.

1,2-dibromotetrachloroethane: An ozone-friendly reagent for the in situ Ramberga-Baecklund rearrangement and its use in the formal synthesis of E-resveratrol

Dibromotetrachloroethane (C2Br2Cl4) is demonstrated as a halogenating reagent for the one-pot conversion of sulfones to alkenes by way of the Ramberga-Baecklund rearrangement. Dibromotetrachloroethane successfully replaces known ozone depleting agents CCl4, CBr2F2 and C2Br 2F4. A formal synthesis of E-resveratrol is demonstrated using C2Br2Cl4.