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(5E)-5-5-chloro-2-[(3-methylbenzyl)oxy]benzylidene-2-thioxo-1,3-thiazolidin-4-one is a thiazolidin-4-one derivative characterized by a benzylidene and thioxo functional group. It features a chloro substituent and a methylbenzyl ether group attached to the benzylidene moiety. This chemical compound demonstrates potential biological activity and is under investigation for its pharmacological properties, which include anti-inflammatory and antimicrobial effects. Its unique chemical structure positions it as a promising lead compound in medicinal chemistry for the development of new drugs. Further research is necessary to fully comprehend its therapeutic potential and possible side effects.

6588-19-8

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6588-19-8 Usage

Uses

Used in Pharmaceutical Industry:
(5E)-5-5-chloro-2-[(3-methylbenzyl)oxy]benzylidene-2-thioxo-1,3-thiazolidin-4-one is used as a lead compound for the development of new drugs due to its potential biological activity and pharmacological properties, such as anti-inflammatory and antimicrobial effects. Its unique chemical structure makes it a valuable candidate for creating novel therapeutic agents.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (5E)-5-5-chloro-2-[(3-methylbenzyl)oxy]benzylidene-2-thioxo-1,3-thiazolidin-4-one serves as a subject of study for understanding its pharmacological properties and potential applications. (5E)-5-5-chloro-2-[(3-methylbenzyl)oxy]benzylidene-2-thioxo-1,3-thiazolidin-4-one's structure and functional groups contribute to its potential as a therapeutic agent, warranting further investigation into its efficacy and safety.
Used in Anti-Inflammatory Applications:
(5E)-5-5-chloro-2-[(3-methylbenzyl)oxy]benzylidene-2-thioxo-1,3-thiazolidin-4-one is used as an anti-inflammatory agent for its potential to alleviate inflammation and associated symptoms. Its pharmacological properties make it a candidate for the treatment of various inflammatory conditions, pending further research into its effectiveness and side effects.
Used in Antimicrobial Applications:
(5E)-5-5-chloro-2-[(3-methylbenzyl)oxy]benzylidene-2-thioxo-1,3-thiazolidin-4-one is also used as an antimicrobial agent, leveraging its potential to combat microbial infections. (5E)-5-5-chloro-2-[(3-methylbenzyl)oxy]benzylidene-2-thioxo-1,3-thiazolidin-4-one's ability to exhibit antimicrobial effects positions it as a possible alternative or addition to existing treatments, particularly in cases where resistance to current antibiotics is a concern. Further research is required to determine its full potential in this application.

Check Digit Verification of cas no

The CAS Registry Mumber 6588-19-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,8 and 8 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6588-19:
(6*6)+(5*5)+(4*8)+(3*8)+(2*1)+(1*9)=128
128 % 10 = 8
So 6588-19-8 is a valid CAS Registry Number.

6588-19-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name benzylphosphonothioic dichloride

1.2 Other means of identification

Product number -
Other names Benzylphosphonthiosaeuredichlorid

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:6588-19-8 SDS

6588-19-8Relevant academic research and scientific papers

Nucleophilic Substitution in Benzylic Thiophosphinyl and Thiophosphonyl Chlorides: the Contribution of Elimination-Addition Pathways with Methylenethiooxophosphorane (Thiophosphene) Intermediates

Coogan, Michael P.,Harger, Martin J. P.

, p. 2101 - 2108 (2007/10/02)

For the reactions of ArCH2P(S)(Ph)Cl and ArCH2P(S)(NMe2)Cl with Et2NH, changing ArCH2 from benzyl to 4-nitrobenzyl increases the rates of substitution by factors of 80 and >103, respectively, and reduces markedly the ability to discriminate bet

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