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1-ethyl-2-[(1E,3Z)-3-(1-ethylquinolin-2(1H)-ylidene)prop-1-en-1-yl]quinolinium is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15185-48-5

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15185-48-5 Usage

Molecular Structure

1-ethyl-2-[(1E,3Z)-3-(1-ethylquinolin-2(1H)-ylidene)prop-1-en-1-yl]quinolinium consists of two quinoline rings connected by a propenyl group with a 1-ethylquinolin-2(1H)-ylidene substituent.

Quinolinium Derivative

It is a derivative of quinolinium compounds.

Potential Applications

The compound has potential applications in pharmaceutical research and other industries.

Further Investigation

Its precise properties and uses would require further investigation and analysis.

Complex Structure

The compound has a complex molecular structure, which may contribute to its unique properties and potential applications.

Check Digit Verification of cas no

The CAS Registry Mumber 15185-48-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,1,8 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 15185-48:
(7*1)+(6*5)+(5*1)+(4*8)+(3*5)+(2*4)+(1*8)=105
105 % 10 = 5
So 15185-48-5 is a valid CAS Registry Number.

15185-48-5SDS

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 1,1'-diethyl-2,2'-quinocarbocyanine iodide

1.2 Other means of identification

Product number -
Other names 1,1'-diethyl-2,2'-carbocyanine 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:15185-48-5 SDS

15185-48-5Relevant academic research and scientific papers

Solid-phase catch, activate, and release synthesis of cyanine dyes

Mason, Stephen J.,Balasubramanian, Shankar

, p. 4261 - 4264 (2002)

(equation presented) Trimethine cyanine dye was synthesized by capture and activation of a hemicyanine intermediate on sulfonyl chloride resin followed by reaction and concomitant cleavage by a heterocyclic carbon nucleophile. A small array of dyes were synthesized and characterized to demonstrate the versatility of this chemistry for a number of hemicyanines and heterocyclic nucleophiles.

MACROPHAGE IDENTIFICATION AGENT, AND IDENTIFICATION METHOD, SORTING METHOD, EVALUATION METHOD, SCREENING METHOD AND KIT USING THE MACROPHAGE IDENTIFIER AGENT

-

Paragraph 0363, (2016/02/28)

An object of the present invention is to provide an identification method for a macrophage subtype using an organic compound. Another object of the present invention is to provide a macrophage identification agent containing an organic compound in which a spectral characteristic obtained when the organic compound is added is different depending on a macrophage subtype. Still another object of the present invention is to provide an evaluation method for a macrophage subtype using a macrophage identification agent, an analysis method for correlation between a macrophage subtype and a test substance, a screening method for correlation between a macrophage subtype and a test substance, and a kit. An identification method for a macrophage subtype utilizing that a spectral characteristic obtained with an organic compound added is different depending on a macrophage subtype is provided.

CONDENSATION OF VILSMEIER COMPLEXES WITH HETEROCYCLIC COMPOUNDS. SYNTHESIS OF CARBOCYANINES

Makin, S. M.,Pomogaev, A. I.

, p. 1916 - 1918 (2007/10/02)

Carbocyanine dyes are formed in the reaction of the quaternary salts of heterocyclic bases containing an active methyl group with the complexes of carboxamides and phosphorus oxychloride.A series of carbocyanines were synthesized, including those containing various substituents at the meso position of the trimethine chain.

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