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4-(2-Anilinovinyl)-1-ethylquinolinium iodide is a quinolinium salt with unique chemical properties and a fluorescent nature, making it a versatile compound for various applications in medicinal chemistry, pharmaceutical research, and as a staining agent in biological and medical imaging.

19487-71-9

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19487-71-9 Usage

Uses

Used in Organic Synthesis:
4-(2-Anilinovinyl)-1-ethylquinolinium iodide is used as a reagent in the synthesis of various organic compounds, facilitating the formation of new chemical entities for research and development.
Used as a Catalyst:
In certain chemical reactions, 4-(2-Anilinovinyl)-1-ethylquinolinium iodide is used as a catalyst to enhance the rate of reaction and improve the efficiency of the process.
Used in Medicinal Chemistry and Pharmaceutical Research:
Due to its unique chemical structure, 4-(2-Anilinovinyl)-1-ethylquinolinium iodide is used as a starting material or intermediate in the development of new drugs and pharmaceuticals.
Used as a Fluorescent Dye in Biological and Medical Imaging:
4-(2-Anilinovinyl)-1-ethylquinolinium iodide is used as a staining agent in biological and medical imaging, providing visual contrast and aiding in the detection and analysis of various biological processes and structures.
Used in Antimicrobial and Antifungal Drug Development:
Possessing potential antimicrobial and antifungal properties, 4-(2-Anilinovinyl)-1-ethylquinolinium iodide is used in the research and development of new drugs and treatments for infectious diseases.
Used in Various Industries:
4-(2-Anilinovinyl)-1-ethylquinolinium iodide's versatility extends its applications across different industries, including but not limited to pharmaceuticals, diagnostics, and materials science, where it can be employed for various purposes based on its chemical and physical properties.

Check Digit Verification of cas no

The CAS Registry Mumber 19487-71-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,4,8 and 7 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 19487-71:
(7*1)+(6*9)+(5*4)+(4*8)+(3*7)+(2*7)+(1*1)=149
149 % 10 = 9
So 19487-71-9 is a valid CAS Registry Number.
InChI:InChI=1/C19H18N2.HI/c1-2-21-15-13-16(18-10-6-7-11-19(18)21)12-14-20-17-8-4-3-5-9-17;/h3-15H,2H2,1H3;1H

19487-71-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[2-(1-ethylquinolin-1-ium-4-yl)ethenyl]aniline,iodide

1.2 Other means of identification

Product number -
Other names -

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:19487-71-9 SDS

19487-71-9Relevant academic research and scientific papers

An effective minor groove binder as a red fluorescent marker for live-cell DNA imaging and quantification

Peng, Xiaojun,Wu, Tong,Fan, Jiangli,Wang, Jingyun,Zhang, Si,Song, Fengling,Sun, Shiguo

supporting information; experimental part, p. 4180 - 4183 (2011/07/07)

Seeing red: DEAB-TO-3 shows a large fluorescence enhancement upon binding to native DNA and a distinct selectivity for double-stranded DNA over total RNA. As a red fluorescent live-cell-permeant DNA minor groove binder, DEAB-TO-3 is promising for highly sensitive DNA detection in vitro and nucleus-specific imaging and DNA quantification in vivo (see picture). Copyright

AMIDINES. PART X. RATES OF REACTION ON N,N'-DIPHENYLFORMAMIDINES WITH N-ALKYLLEPIDINIUM IODIDES

Oszczapowicz, Janusz,Orlinski, Ryszard,Jaroszewska, Jolanta,Kaminska, Elzbieta

, p. 725 - 734 (2007/10/02)

The specific rates of reaction of eleven symmetrically meta or para disubstituted N,N'-diphenylformamidines with N-ethyl- and N-methyl-lepidinium iodides have been compared and attempts at correlating with Hammett's ? constants of substituents at phenyl rings have been made.The results were compared with those obtained previously for reaction with N-alkylquinaldinium iodides.It has been observed that reactivity order of N-alkylmethylquinolinium iodides is reversed when the sign of inductive effect of substituents in formamidines is changed.The influence of substitution in molecules of both substrates on reaction rate is discussed.The influence of salts added to the reaction medium and decrease in reaction rate with increase in basicity has been observed.Unreported 21 hemicyanine dyes have been synthesized.

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