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The chemical compound "5-[(3-cyclopentyl-4-oxo-2-thioxo-1,3-thiazolidin-5-ylidene)methyl]-1-ethyl-6-[4-(4-fluorophenyl)piperazin-1-yl]-4-methyl-2-oxo-1,2-dihydropyridine-3-carbonitrile" is a complex organic molecule with a molecular formula of C31H31FN6O3S2. It features a pyridine ring with various functional groups, including a carbonitrile group, a cyclopentyl-thiazolidinone moiety, an ethyl group, a piperazine ring with a 4-fluorophenyl substituent, and a methyl group. 5-[(3-cyclopentyl-4-oxo-2-thioxo-1,3-thiazolidin-5-ylidene)methyl]-1-ethyl-6-[4-(4-fluorophenyl)piperazin-1-yl]-4-methyl-2-oxo-1,2-dihydropyridine-3-carbonitrile is characterized by its unique structure and potential pharmacological properties, which may be relevant in the development of new drugs or chemical research.

7063-92-5

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7063-92-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7063-92-5 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, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7063-92:
(6*7)+(5*0)+(4*6)+(3*3)+(2*9)+(1*2)=95
95 % 10 = 5
So 7063-92-5 is a valid CAS Registry Number.

7063-92-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-[(3-cyclopentyl-4-oxo-2-sulfanylidene-1,3-thiazolidin-5-ylidene)methyl]-1-ethyl-6-[4-(4-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

1.5 Emergency phone number

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More Details:7063-92-5 SDS

7063-92-5Downstream Products

7063-92-5Relevant academic research and scientific papers

AN IMPROVED PROCEDURE FOR THE PREPARATION OF 2-ISOXAZOLINES

Larsen, Karl Erik,Torssell, Kurt B. G.

, p. 2985 - 2988 (2007/10/02)

Aldoximes were converted in high yields by N-Chlorosuccinimide into hydroxamic acid chlorides, and corresponding nitrile oxides generated by addition of triethylamine at 40-50 deg C underwent 1,3-dipolar addition to alkenes, giving 2-isoxazolines.The whole procedure could be performed as a one-pot reaction.Oximes with other functions, sensitive to free chlorine could be converted selectively into hydroxamic acid chlorides by this procedure.Isopropylidene glyceraldoxime was added to acrolein diethylacetal thus affording an entrance to carbohydrate synthesis but the stereospecificity of the reaction is low. 2:3, 5:6-Di-O-isopropylidene-D- mannose oxime was converted to the N-hydroximinolactone by treatment with NCS and base.

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