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1H-Imidazolium, 1-ethenyl-3-ethyl-, iodide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

34254-21-2

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34254-21-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34254-21-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,2,5 and 4 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 34254-21:
(7*3)+(6*4)+(5*2)+(4*5)+(3*4)+(2*2)+(1*1)=92
92 % 10 = 2
So 34254-21-2 is a valid CAS Registry Number.

34254-21-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-ethenyl-3-ethyl-1,2-dihydroimidazol-1-ium,iodide

1.2 Other means of identification

Product number -
Other names 3-Ethyl-1-vinylimidazoliumjodid

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:34254-21-2 SDS

34254-21-2Downstream Products

34254-21-2Relevant academic research and scientific papers

Photogenerated lophyl radicals in 1-alkyl-3-vinylimidazolium bis(trifluoromethylsulfonyl)imides

Berdzinski, Stefan,Strehmel, Bernd,Strehmel, Veronika

, p. 714 - 725 (2015)

1-Alkyl-3-vinylimidazolium bis(trifluoromethylsulfonyl)imides were investigated as a matrix for photogenerated lophyl radicals obtained by irradiation of o-chlorohexaarylbisimidazole (o-Cl-HABI). Photoinduced polymerization of ionic liquid monomers using the photoinitiator system composed of o-Cl-HABI and 3-mercapto-1,2,4-4H-triazole was investigated by photo-DSC. Selected thermal properties and viscosity of these ionic liquid monomers are important to understand the lophyl radical kinetics after exposure. Solvent cage effects and viscosity of the ionic liquid monomers strongly affect radical recombination in the dark. This was investigated at different temperatures. The rate constant for radical recombination (krec) decreases from the methyl to the butyl substituted ionic liquid monomer. This may be attributed to an increasing viscosity with increasing size of the alkyl substituent. However, further increase in the size of the alkyl substituent from a butyl to a heptyl group bound at the imidazolium ion results in an increase of krec although the viscosity does further increase. Therefore, a minimum in krec was found for the butyl substituted ionic liquid monomer. Furthermore, the Eyring parameters indicated a dependence on the chain length of the alkyl substituent bound at the imidazolium ion while the activation energy of the viscous flow only slightly changes. Furthermore, the size of the alkyl substituent bound at the cation of the ionic liquid monomers strongly influences both solvent cage and viscosity, and therefore, the concentration of lophyl radicals during photoinduced generation. Photo-induced polymerization of the ionic liquid monomers is affected by viscosity at low conversion and by vitrification at higher conversion. The latter is important for application of the ionic liquid monomers and the polymers made from them by photoinduced polymerization.

A facile four component one-pot synthesis of polyhydroquinoline derivatives catalyzed by ionic liquid via modified Hantzsch reaction

Nirmal, Jay P.,Dadhaniya, Pratish V.,Patel, Manish P.,Patel, Ranjan G.

experimental part, p. 587 - 592 (2011/01/04)

An efficient and newer Hantzsch reaction for the synthesis of polyhydroquinoline derivatives have been reported via fourcomponent condensation of aldehydes, cyclic 1,3-diketones, β-keto esters, NH4OAc and catalytic amount of ionic liquid 1-Viny

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