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(5E)-5-(3-iodo-5-methoxy-4-{2-[2-(prop-2-en-1-yl)phenoxy]ethoxy}benzylidene)-3-methyl-2-thioxo-1,3-thiazolidin-4-one is a complex organic compound with a molecular formula of C23H21IO4S. It is characterized by a 1,3-thiazolidin-4-one core structure, which features a 5-membered ring with a sulfur atom and a ketone group. The molecule contains a 3-iodo-5-methoxy substituted benzylidene group, which is connected to the thiazolidinone ring through a double bond (E configuration). Additionally, it has a 2-[2-(prop-2-en-1-yl)phenoxy]ethoxy substituent attached to the benzene ring, providing a phenolic and allyl group. (5E)-5-(3-iodo-5-methoxy-4-{2-[2-(prop-2-en-1-yl)phenoxy]ethoxy}benzylidene)-3-methyl-2-thioxo-1,3-thiazolidin-4-one is likely to be found in the field of pharmaceuticals or chemical research due to its intricate structure and potential for various applications.

6188-74-5

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6188-74-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6188-74-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,8 and 8 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6188-74:
(6*6)+(5*1)+(4*8)+(3*8)+(2*7)+(1*4)=115
115 % 10 = 5
So 6188-74-5 is a valid CAS Registry Number.

6188-74-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (2E,4E)-5-(dimethylamino)-3-methylpenta-2,4-dienenitrile

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

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More Details:6188-74-5 SDS

6188-74-5Relevant academic research and scientific papers

Photoreactive polymer brushes for high-density patterned surface derivatization using a diels-alder photoclick reaction

Arumugam, Selvanathan,Orski, Sara V.,Locklin, Jason,Popik, Vladimir V.

, p. 179 - 182 (2012)

Reactive polymer brushes grown on silicon oxide surfaces were derivatized with photoreactive 3-(hydroxymethyl)naphthalene-2-ol (NQMP) moieties. Upon 300 or 350 nm irradiation, NQMP efficiently produces o-naphthoquinone methide (oNQM), which in turn undergoes very rapid Diels-Alder addition to vinyl ether groups attached to a substrate, resulting in the covalent immobilization of the latter. Any unreacted oNQM groups rapidly add water to regenerate NQMP. High-resolution surface patterning is achieved by irradiating NQMP-derivatized surfaces using photolithographic methods. The Diels-Alder photoclick reaction is orthogonal to azide-alkyne click chemistry, enabling sequential photoclick/azide-click derivatizations to generate complex surface functionalities.

SYNTHESIS OF THE VINYL PROPARGYL DIETHERS OF DIOLS UNDER CONDITIONS OF PHASE-TRANSFER CATALYSIS

Lavrov, V. I.,Parshina, L. N.,Stankevich, V. K.,Trofimov, B. A.

, p. 249 - 251 (2007/10/02)

A method was developed for the synthesis of the vinyl propargyl diethers of diols from the vinyl monoethers of diols and propargyl halides under the conditions of phase-transfer catalysis.

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