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3-METHYL-4-PHENYLTHIAZOLINE-2-THIONE, also known as MPTT, is a heterocyclic chemical compound with the molecular formula C9H7NS. It is a thiazoline derivative that has been studied for its potential pharmacological properties, including its ability to scavenge free radicals and protect against oxidative stress. 3-METHYL-4-PHENYLTHIAZOLINE-2-THIONE has also been investigated for its potential use as a herbicide and has been evaluated for its antifungal and antibacterial properties, making it a compound of interest for various industrial and medical applications.

21402-19-7

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21402-19-7 Usage

Uses

Used in Pharmaceutical Industry:
3-METHYL-4-PHENYLTHIAZOLINE-2-THIONE is used as a pharmaceutical candidate for its potential pharmacological properties, such as its ability to scavenge free radicals and protect against oxidative stress. This makes it a promising compound for the development of drugs targeting various health conditions related to oxidative stress.
Used in Agriculture:
3-METHYL-4-PHENYLTHIAZOLINE-2-THIONE is used as a potential herbicide, as it has been investigated for its ability to control the growth of unwanted plants. Its herbicidal properties could be utilized in the development of new and effective herbicides for agricultural applications.
Used in Antimicrobial Applications:
3-METHYL-4-PHENYLTHIAZOLINE-2-THIONE is used as an antimicrobial agent for its antifungal and antibacterial properties. It can be employed in the development of new antimicrobial agents to combat various microbial infections in both medical and industrial settings.
Used in Industrial Applications:
3-METHYL-4-PHENYLTHIAZOLINE-2-THIONE is used in various industrial applications due to its unique chemical properties. Its potential use in the development of new materials, coatings, or other industrial products can be explored, taking advantage of its ability to scavenge free radicals and protect against oxidative stress.

Check Digit Verification of cas no

The CAS Registry Mumber 21402-19-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,4,0 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 21402-19:
(7*2)+(6*1)+(5*4)+(4*0)+(3*2)+(2*1)+(1*9)=57
57 % 10 = 7
So 21402-19-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H9NS2/c1-11-9(7-13-10(11)12)8-5-3-2-4-6-8/h2-7H,1H3

21402-19-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-4-phenyl-1,3-thiazole-2-thione

1.2 Other means of identification

Product number -
Other names methyl-4-phenylthiazoline-2-thione

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:21402-19-7 SDS

21402-19-7Relevant academic research and scientific papers

Synthesis and Evaluation of 2(3H)-Thiazole Thiones as Tyrosinase Inhibitors

Emami, Saeed,Hosseinimehr, Seyed Jalal,Shahrbandi, Kami,Enayati, Ahmad Ali,Esmaeeli, Zahra

, p. 629 - 637 (2012/09/22)

A series of 2(3H)-thiazole thiones 3-5 was synthesized and evaluated for tyrosinase inhibition and DPPH radical scavenging activities. Among them, 3-methyl-4-phenyl-2(3H)-thiazole thione (4a) showed good tyrosinase inhibitory activity, even better than that of the well-known tyrosinase inhibitor, namely, kojic acid. From the structure-activity point of view, although it was found that the phenolic hydroxyl group in prototype 3-5 might contribute to the scavenging activity against DPPH radicals, there was no correlation between the potency of tyrosinase inhibition and the presence of the phenolic moiety. The in silico ADME-Tox screening revealed that the drug-likeness and drug-score values of the most potent compound 4a were significantly higher than those of kojic acid. Copyright

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