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The chemical compound "5-{[3-(1,1-dioxidotetrahydrothiophen-3-yl)-4-oxo-2-thioxo-1,3-thiazolidin-5-ylidene]methyl}-1-ethyl-6-[4-(2-fluorophenyl)piperazin-1-yl]-4-methyl-2-oxo-1,2-dihydropyridine-3-carbonitrile" is a complex organic molecule with a long and intricate structure. It features a pyridine ring system, which is a six-membered aromatic ring containing two nitrogen atoms. The compound also includes a 1,3-thiazolidine ring, a heterocyclic ring with sulfur and nitrogen atoms, and a piperazine ring, which is a six-membered ring with two nitrogen atoms. The molecule contains various functional groups, such as carbonitrile, oxo, and fluorophenyl groups, which contribute to its overall properties and potential applications. Due to its complexity, 5-{[3-(1,1-dioxidotetrahydrothiophen-3-yl)-4-oxo-2-thioxo-1,3-thiazolidin-5-ylidene]methyl}-1-ethyl-6-[4-(2-fluorophenyl)piperazin-1-yl]-4-methyl-2-oxo-1,2-dihydropyridine-3-carbonitrile may have specific uses in pharmaceuticals, agrochemicals, or other specialized fields, but its exact application would depend on its specific properties and the context in which it is being used.

7063-89-0

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7063-89-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7063-89-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,6 and 3 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7063-89:
(6*7)+(5*0)+(4*6)+(3*3)+(2*8)+(1*9)=100
100 % 10 = 0
So 7063-89-0 is a valid CAS Registry Number.

7063-89-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-[[3-(1,1-dioxothiolan-3-yl)-4-oxo-2-sulfanylidene-1,3-thiazolidin-5-ylidene]methyl]-1-ethyl-6-[4-(2-fluorophenyl)piperazin-1-yl]-4-methyl-2-oxopyridine-3-carbonitrile

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

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More Details:7063-89-0 SDS

7063-89-0Downstream Products

7063-89-0Relevant academic research and scientific papers

An improved method for preparation of nitrile oxides from nitroalkanes for in situ dipolar cycloadditions

Basel, Yochai,Hassner, Alfred

, p. 309 - 312 (2007/10/03)

A new method has been found for generation of nitrile oxides in situ from nitroalkanes under mild conditions. Thus, reaction of nitroalkanes 1 with di-tert-butyl dicarbonate (2) and 4-dimethylaminopyridine (3) as catalyst in the presence of dipolarophiles

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