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13041-79-7

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13041-79-7 Usage

General Description

4-Cyanostilbene, also known as 4-methyl-4'-cyanostilbene, is a molecule consisting of a central stilbene core with a cyanide group attached at one of the phenyl rings. It is a fluorescent compound with potential applications in organic electronics, such as organic light-emitting diodes (OLEDs) and organic photovoltaic devices. It has also been studied for its potential use as a photoinitiator for polymerization reactions. 4-Cyanostilbene is a versatile chemical that has been investigated for its optical and electronic properties, making it a promising candidate for various technological and industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 13041-79-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,4 and 1 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 13041-79:
(7*1)+(6*3)+(5*0)+(4*4)+(3*1)+(2*7)+(1*9)=67
67 % 10 = 7
So 13041-79-7 is a valid CAS Registry Number.
InChI:InChI=1/C15H11N/c16-12-15-10-8-14(9-11-15)7-6-13-4-2-1-3-5-13/h1-11H

13041-79-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Cyanostilbene

1.2 Other means of identification

Product number -
Other names 4-(2-phenylethenyl)benzonitrile

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:13041-79-7 SDS

13041-79-7Relevant articles and documents

A soluble fluorous palladium complex that promotes heck reactions and can be recovered and reused

Curran, Dennis P.,Fischer, Karin,Moura-Letts, Gustavo

, p. 1379 - 1382 (2004)

A new fluorous SCS pincer palladium complex is synthesized and shown to efficiently promote typical Heck reactions under microwave or thermal heating. The complex is air stable and can be recovered after reactions for reuse by fluorous solid phase extraction. By analogy to related complexes, it may function as a precursor of soluble ligandless palladium metal.

Combination of palladium and oleic acid coated-magnetite particles: Characterization and using in Heck coupling reaction with magnetic recyclability

Rafiee, Ezzat,Ataei, Ali,Nadri, Shirin,Joshaghani, Mohammad,Eavani, Sara

, p. 302 - 309 (2014)

The magnetic Fe3O4 nanoparticles were prepared by co-precipitation method and coated with oleic acid. The oleic acid coated Fe3O4 (Fe@OA) particles were used for the immobilization of palladium particles to prod

Acetylferrocenyloxime palladacycle-catalyzed Heck reactions

Iyer, Suresh,Jayanthi, A

, p. 7877 - 7878 (2001)

Acetylferrocenyloxime palladacycle catalyzed the Heck reaction of aryl bromides and activated aryl chlorides.

Synthesis and characterization of Pd(II) complexes bearing NS, CS, SNS and SCS ligands. Evaluation of their microwave assisted catalytic activity in C–C coupling reactions

Aguilar-Castillo, Bethsy A.,Gabriel Flores-Rojas, G.,González-Sebastián, Lucero,Hernández-Ortega, Simón,Morales-Morales, David,Reyes-Martínez, Reyna

, (2020)

A series of coordination (Pd-NS, Pd-SNS, Pd-SNS-O) and organometallic (Pd-C and Pd-SCS) Pd(II) complexes supported by bidentate and tridentate ligands featuring sulphur moieties have been prepared. All ligands and their palladium complexes were fully char

Pd supported on clicked cellulose-modified magnetite-graphene oxide nanocomposite for C-C coupling reactions in deep eutectic solvent

Karimi, Sabah,Masteri-Farahani, Majid,Niakan, Mahsa,Shekaari, Hemayat

, (2020/10/02)

Cellulose-modified magnetite-graphene oxide nanocomposite was prepared via click reaction and utilized for immobilization of palladium (Pd) nanoparticles without using additional reducing agent. The abundant OH groups of cellulose provided the uniform dispersion and high stability of Pd nanoparticles, while magnetite-graphene oxide as a supporting material offered high specific surface area and easy magnetic separation. The as-prepared nanocomposite served as a heterogeneous catalyst for the Heck and Sonogashira coupling reactions in various hydrophilic and hydrophobic deep eutectic solvents (DESs) as sustainable and environmentally benign reaction media. Among the fifteen DESs evaluated for coupling reactions, the hydrophilic DES composed of dimethyl ammonium chloride and glycerol exhibited the best results. Due to the low miscibility of catalyst and DES in organic solvents, the separated aqueous phase containing both of the catalyst and DES can be readily recovered by evaporating water and retrieved eight times with negligible loss of catalytic performance.

Introduction of a Recyclable Basic Ionic Solvent with Bis-(NHC) Ligand Property and The Possibility of Immobilization on Magnetite for Ligand- and Base-Free Pd-Catalyzed Heck, Suzuki and Sonogashira Cross-Coupling Reactions in Water

Min, Qingwang,Miao, Penghua,Chu, Deyu,Liu, Jinghan,Qi, Meijuan,Kazemnejadi, Milad

, p. 3030 - 3047 (2021/02/16)

A new versatile and recyclable NHC ligand precursor has been developed with ligand, base, and solvent functionalities for the efficient Pd-catalyzed Heck, Suzuki and Sonogashira cross-coupling reactions under mild conditions. Furthermore, NHC ligand precursor was immobilized on magnetite and its catalytic activity was also evaluated towards the coupling reactions as a heterogeneous catalyst. The NHC ligand precursor was prepared with imidazolium functionalization of TCT followed by a simple ion exchange by hydroxide ions. However, the results revealed an excellent catalytic activity for the both homogeneous and heterogeneous catalytic systems. 1.52?g.cm?3 and 1194 cP was obtained for the density and viscosity of the NHC ligand precursor respectively. On the other hand, the heterogeneous type could be readily recovered from the reaction mixture and reused for several times while preserving its properties. Heterogeneous nature of the magnetic catalyst was studied by hot filtration, mercury poisoning, and three-phase tests. High to excellent yields were obtained for all entries for the both homogeneous and heterogeneous catalysts, which reflects the high consistency of the catalyst. Graphic Abstract: [Figure not available: see fulltext.]

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