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2-(9H-Carbazol-9-yl)ethyl acrylate (PCz) is an acrylate-based conducting polymer that features a carbazole group as an electron-donating pendant. This polymer is known for its high charge carrier mobility, photochemical stability, and excellent thermal and electroluminescent properties, making it a valuable material for various applications in the field of organic electronics.

6915-68-0

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6915-68-0 Usage

Uses

Used in Organic Electronics:
2-(9H-Carbazol-9-yl)ethyl acrylate 97 is used as a charge transporting material for its high charge carrier mobility and photochemical stability, making it suitable for applications in organic electronics.
Used in Organic Light Emitting Diodes (OLEDs):
In the OLED industry, 2-(9H-Carbazol-9-yl)ethyl acrylate 97 is used as a key component in the fabrication of organic light emitting diodes due to its high electroluminescent properties.
Used in Photovoltaic Cells:
2-(9H-Carbazol-9-yl)ethyl acrylate 97 is utilized as a conducting polymer in the production of photovoltaic cells, taking advantage of its high charge carrier mobility and thermal properties.
Used in Memory Based Devices:
In the memory industry, 2-(9H-Carbazol-9-yl)ethyl acrylate 97 is used as a conducting polymer to enhance the performance and stability of memory-based devices, capitalizing on its high charge carrier mobility and thermal properties.

Check Digit Verification of cas no

The CAS Registry Mumber 6915-68-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,1 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6915-68:
(6*6)+(5*9)+(4*1)+(3*5)+(2*6)+(1*8)=120
120 % 10 = 0
So 6915-68-0 is a valid CAS Registry Number.
InChI:InChI=1/C17H15NO2/c1-2-17(19)20-12-11-18-15-9-5-3-7-13(15)14-8-4-6-10-16(14)18/h2-10H,1,11-12H2

6915-68-0 Well-known Company Product Price

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  • Aldrich

  • (570362)  2-(9H-Carbazol-9-yl)ethylacrylate  97%

  • 6915-68-0

  • 570362-1G

  • 5,201.82CNY

  • Detail

6915-68-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-carbazol-9-ylethyl prop-2-enoate

1.2 Other means of identification

Product number -
Other names 2-(9H-Carbazol-9-yl)ethyl acrylate

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:6915-68-0 SDS

6915-68-0Downstream Products

6915-68-0Relevant academic research and scientific papers

Neutral state colorless electrochromic polymer networks: Spacer effect on electrochromic performance

Gulfidan, Damla,Sefer, Emre,Koyuncu, Sermet,Acar, Metin H.

, p. 5998 - 6005 (2015/01/09)

A series of carbazole-based monomers and their corresponding polymers with various spacer units were synthesized and coated onto ITO-glass surface via an electrochemical cross-linking process. All carbazole-based polymers exhibited multi-electrochromic be

Microstructure characterization of poly(2-N-carbazolylethyl acrylate) by two-dimensional NMR spectroscopy

Brar,Markanday,Gandhi

, p. 58 - 63 (2007/10/03)

Poly(2-N-carbazolylethyl acrylate) has been synthesized by solution polymerization of 2-N-carbazolyethyl acrylate with 2,2′- azobisisobutyronitrile as free radical initiator. Distortionless Enhancement by Polarization Transfer has been used to distinguish between the overlapping main-chain methine and side-chain methylene resonances in 13C( 1H) NMR spectrum. Configurational assignments of carbon and proton resonances of main-chain methylene group have been done using two-dimensional Heteronuclear Single Quantum Correlation spectroscopy and two-dimensional Total Correlation Spectroscopy. Two and three bond order carbon/proton couplings have been investigated using Heteronuclear Multiple Bond Correlation studies.

Electron-Transfer Quenching Accompanied by Highly Efficient Energy Migration in Polymer Langmuir-Blodgett Films

Yatsue, Toru,Miyashita, Tokuji

, p. 16047 - 16051 (2007/10/02)

Copolymers of N-dodecylacrylamide (DDA), which has the excellent property to form LB film, and 2-(9-carbazolyl)ethyl acrylate (CzEA) with various copolymer compositions were prepared to investigate the electron transfer quenching of the excited carbazole chromophore in LB film assembly.The copolymers form a stable condensed monolayer and LB film in a wide range of copolymer compositions.In LB films, the emission spectra show only the structured emission characteristic of the monomeric carbazole chromophore at 350 nm and no excimer emission whereas the corresponding N-vinylcarbazole copolymer LB films in the previous study show strong emision from excimer which acts as an energy trapping site.For the quenching study, the DDA-CzEA monolayer are in direct contact with the mixed monolayer of barius stearate and stearyl viologen quencher.The emission of the excited carbazole was quenched effectively by a small amount of the viologen quencher in the mixed monolayer.The quenching efficiency was varied linearly by the mole fraction of carbazole chromophore in the copolymer monolayer.The effective electron-transfer quenching is attributed to the highly efficient energy migration between carbazole chromophores, which is assisted with a regular alignment of carbazole chromophore and no excimer formation in the copolymer LB films.The plots of ln(I0/I-1) (I in the presence of and I0 in the absence of the quencher) vs distance (R) between the quenchers gave a linear relationship.The mechanism of electron transfer quenching in the LB film assembly is discussed on the basis of electron-tunneling and energy migration.

A NOVEL SYNTHESIS OF POLYACRYLATES AND POLYMETHACRYLATES WITH PENDANT CARBAZOLE GROUPS

Strohriegl, Peter

, p. 261 - 267 (2007/10/02)

A series of novel polyacrylates and polymethacrylates with pendant carbazole groups has been prepared.In these polymers the carbazole groups are separated from the polymer backbone by alkyl spacers of variable length.The title compounds have been prepared by two different methods: free radical polymerization of the corresponding acrylates and methacrylates and a novel polymeranalogous reaction of ω-hydroxyalkylcarbazoles with poly(meth)acryloylchloride.

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