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6-METHOXY-N-ETHYLQUINOLINIUM IODIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

34373-76-7

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34373-76-7 Usage

Uses

MEQ is a cell membrane impermeable chloride indicator..

Check Digit Verification of cas no

The CAS Registry Mumber 34373-76-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,3,7 and 3 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 34373-76:
(7*3)+(6*4)+(5*3)+(4*7)+(3*3)+(2*7)+(1*6)=117
117 % 10 = 7
So 34373-76-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H14NO.HI/c1-3-13-8-4-5-10-9-11(14-2)6-7-12(10)13;/h4-9H,3H2,1-2H3;1H/q+1;/p-1

34373-76-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-ethyl-6-methoxyquinolin-1-ium,iodide

1.2 Other means of identification

Product number -
Other names 1-ethyl-6-methoxy-quinolinium,iodide

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:34373-76-7 SDS

34373-76-7Relevant academic research and scientific papers

External Heavy-Atom Effect via Orbital Interactions Revealed by Single-Crystal X-ray Diffraction

Sun, Xingxing,Zhang, Baicheng,Li, Xinyang,Trindle, Carl O.,Zhang, Guoqing

, p. 5791 - 5797 (2016/08/05)

Enhanced spin-orbit coupling through external heavy-atom effect (EHE) has been routinely used to induce room-temperature phosphorescence (RTP) for purely organic molecular materials. Therefore, understanding the nature of EHE, i.e., the specific orbital interactions between the external heavy atom and the luminophore, is of essential importance in molecular design. For organic systems, halogens (e.g., Cl, Br, and I) are the most commonly seen heavy atoms serving to realize the EHE-related RTP. In this report, we conduct an investigation on how heavy-atom perturbers and aromatic luminophores interact on the basis of data obtained from crystallography. We synthesized two classes of molecular systems including N-haloalkyl-substituted carbazoles and quinolinium halides, where the luminescent molecules are considered as "base" or "acid" relative to the heavy-atom perturbers, respectively. We propose that electron donation from a π molecular orbital (MO) of the carbazole to the σ? MO of the C-X bond (π/σ?) and n electron donation to a π? MO of the quinolinium moiety (n/π ?) are responsible for the EHE (RTP) in the solid state, respectively.

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