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4-Phenyl-2-thiazolidinethione is an organosulfur compound characterized by a molecular formula of C9H9NS and a molar mass of 163.24 g/mol. It features a thiazolidine ring fused with a phenyl group, endowing it with potential biological activities such as antioxidant and antidiabetic properties. 4-Phenyl-2-thiazolidinethione is currently under investigation for its therapeutic potential in managing type 2 diabetes and its associated complications.

1908-90-3

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1908-90-3 Usage

Uses

Used in Pharmaceutical Research:
4-Phenyl-2-thiazolidinethione is utilized as a pharmaceutical candidate for its potential role in the treatment of type 2 diabetes. It is recognized for its ability to inhibit lipid peroxidation and enhance insulin sensitivity, which are crucial for managing diabetes and its complications.
Used in Synthesis of Pharmaceutical Compounds:
In the chemical industry, 4-Phenyl-2-thiazolidinethione serves as a valuable building block in the synthesis of various pharmaceutical compounds. Its unique structure and properties make it a versatile component in the development of new drugs with diverse therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1908-90-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,0 and 8 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1908-90:
(6*1)+(5*9)+(4*0)+(3*8)+(2*9)+(1*0)=93
93 % 10 = 3
So 1908-90-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H9NS2/c11-9-10-8(6-12-9)7-4-2-1-3-5-7/h1-5,8H,6H2,(H,10,11)

1908-90-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Phenyl-1,3-thiazolidine-2-thione

1.2 Other means of identification

Product number -
Other names 2-Thiazolidinethione,4-phenyl

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:1908-90-3 SDS

1908-90-3Relevant academic research and scientific papers

Evaluation of pyrrolidin-2-imines and 1,3-thiazolidin-2-imines as inhibitors of nitric oxide synthase

Shankaran,Donnelly, Karla L.,Shah, Shrenik K.,Guthikonda, Ravindra N.,MacCoss, Malcolm,Humes, John L.,Pacholok, Stephen G.,Grant, Stephan K.,Kelly,Wong

, p. 4539 - 4544 (2007/10/03)

Syntheses and evaluation of pyrrolidin-2-imines and 1,3-thiazolidin-2- imines as inhibitors of nitric oxide synthase (NOS) are discussed. An extensive SAR was established for pyrrolidin-2-imines class of compounds. The amidines came out as the most potent inhibitors in addition to displaying selectivity.

STEREOSPECIFIC SYNTHESIS OF THIAZOLIDINE-2-THIONES

Brunet, Ernesto,Carreno, M. Carmen,Ruano, Jose Luis Garcia

, p. 1181 - 1195 (2007/10/02)

The synthesis of thiazolidine-2-thiones from vic-iodoalkanecarbamates, stereospecifically obtained from cis and trans-butene, is reported.Reaction of the iodo-derivatives with potassium ethylxanthate and sodium hydroxide, allowed the stereospecific format

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