127236-58-2

Usage

Uses

Used in Organic Synthesis:
1-(1-P-TOLYL-VINYL)-NAPHTHALENE is used as a building block in organic synthesis for its ability to form a variety of other organic compounds. Its unique structure allows for the creation of diverse chemical products, contributing to the advancement of organic chemistry.
Used as a Fluorescent Dye:
In the field of material science, 1-(1-P-TOLYL-VINYL)-NAPHTHALENE is utilized as a fluorescent dye due to its specific optical properties. Its fluorescence can be harnessed in various applications, such as bioimaging, sensing, and other areas where the detection of light emission is crucial.
Used as a Chemical Intermediate:
1-(1-P-TOLYL-VINYL)-NAPHTHALENE serves as a chemical intermediate in the production of various organic compounds. Its role in the synthesis process is essential for creating a range of products with different applications in various industries.
Used in Organic Electronic Devices:
1-(1-P-TOLYL-VINYL)-NAPHTHALENE is also used as a component in organic electronic devices, such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs), due to its electronic properties and compatibility with other materials in these devices.

InChI:InChI=1/C19H16/c1-14-10-12-16(13-11-14)15(2)18-9-5-7-17-6-3-4-8-19(17)18/h3-13H,2H2,1H3

Upstream product

• 122-00-9 para-methylacetophenone 
• 703-55-9 1-naphthylmagnesiumbromide 
• 13026-12-5 3-(1-naphthyl)propenoic acid 
• 108-88-3 toluene 
• 106-38-7 para-bromotoluene 
• 13026-12-5 (E)-3-(naphthalen-1-yl)acrylic acid 
• 102421-44-3 4-methyl-N'-(1-(naphthalen-1-yl)ethylidene)benzenesulfonohydrazide 
• 941-98-0 1'-naphthacetophenone 
• 4294-57-9 para-methylphenylmagnesium bromide 

Relevant academic research and scientific papers

Synthesis of naphthyl-substituted terminal olefins via Pd-Catalyzed one-pot coupling of acetylnaphthalene, N-Tosylhydrazide with aryl halide

In this study, a one-pot two-step Pd-catalyzed reductive eliminate between acetyl naphthalene derivatives, tosylhydrazide, and aryl halide, affording substituted 1(or 2)-(1-phenylvinyl)naphthalene in moderate-to-excellent yields, was reported. Notably, so

Traceless directing group mediated branched selective alkenylation of unbiased arenes

Owing to the synthetic importance of branched olefinated products, we report palladium catalyzed formation of branched olefins facilitated by a C-H activation based protocol. This involves selective insertion of olefins and subsequent decarboxylation using a completely unbiased benzene ring as the starting precursor. The significance of the protocol has been further highlighted by exhibition of functionality tolerance along with a late-stage modification of the branched olefinated products leading to the formation of other functionalized molecules.

Branched Arylalkenes from Cinnamates: Selectivity Inversion in Heck Reactions by Carboxylates as Deciduous Directing Groups

A decarboxylative Mizoroki–Heck coupling of aryl halides with cinnamic acids has been developed in which the carboxylate group directs the arylation into its β-position before being tracelessly removed through protodecarboxylation. In the presence of a copper/palladium catalyst, both electron-rich and electron-deficient aryl bromides and chlorides bearing numerous functionalities were successfully coupled with broadly available cinnamates, with selective formation of 1,1-disubstituted alkenes. This reaction concept, in which the carboxylate acts as a deciduous directing group, ideally complements traditional 1,2-selective Heck reactions of styrenes.

A ligand free and room temperature protocol for Pd-catalyzed kumada-corriu couplings of unactivated alkenyl phosphates

Kumada - Corriu cross-couplings of nonactivated cyclic and acyclic vinyl phosphates with aryl magnesium reagents afforded a series of 1,1-disubtituted alkenes in good yields for most cases when the reactions were performed at room temperature with the sim

PtBr2-catalyzed consecutive enyne metathesis-aromatization of 1-(1-methoxy-but-3-enyl)-2-(1-alkynyl)benzenes: Dual role of the Pt catalyst

(Chemical Equation Presented) 1,7-Enynes 1, connected through an aromatic ring and bearing a leaving methoxy group at the 4-position, underwent the PtBr2-catalyzed enyne metathesis followed by aromatization in one pot to afford vinyl naphthalen