Welcome to LookChem.com Sign In|Join Free

CAS

  • or

41270-34-2

Post Buying Request

41270-34-2 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

41270-34-2 Usage

Description

(5E)-3-methyl-5-(3-methyl-4-oxo-2-thioxo-1,3-thiazolidin-5-ylidene)-2-thioxo-1,3-thiazolidin-4-one is a complex organic molecule characterized by its thiazolidine ring structure and the presence of multiple functional groups such as a ketone, a thioxo group, and a thiazolidine ring. (5E)-3-methyl-5-(3-methyl-4-oxo-2-thioxo-1,3-thiazolidin-5-ylidene)-2-thioxo-1,3-thiazolidin-4-one holds potential biological activity, as similar thiazolidine derivatives have been investigated for their anti-inflammatory, anti-cancer, and anti-diabetic properties. Further research is essential to explore and confirm the medicinal applications of this compound and its possible derivatives.

Uses

Used in Pharmaceutical Industry:
(5E)-3-methyl-5-(3-methyl-4-oxo-2-thioxo-1,3-thiazolidin-5-ylidene)-2-thioxo-1,3-thiazolidin-4-one is used as a potential therapeutic agent for various medical conditions due to its potential biological activity. (5E)-3-methyl-5-(3-methyl-4-oxo-2-thioxo-1,3-thiazolidin-5-ylidene)-2-thioxo-1,3-thiazolidin-4-one's anti-inflammatory, anti-cancer, and anti-diabetic properties, as observed in related thiazolidine derivatives, make it a promising candidate for pharmaceutical development.
Used in Research and Development:
In the field of scientific research, (5E)-3-methyl-5-(3-methyl-4-oxo-2-thioxo-1,3-thiazolidin-5-ylidene)-2-thioxo-1,3-thiazolidin-4-one serves as a subject of study for understanding its chemical properties, potential interactions with biological systems, and its possible applications in the development of new drugs and therapies. (5E)-3-methyl-5-(3-methyl-4-oxo-2-thioxo-1,3-thiazolidin-5-ylidene)-2-thioxo-1,3-thiazolidin-4-one's structure and functional groups provide a foundation for exploring its reactivity and potential to form new derivatives with enhanced or novel medicinal properties.

Check Digit Verification of cas no

The CAS Registry Mumber 41270-34-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,2,7 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 41270-34:
(7*4)+(6*1)+(5*2)+(4*7)+(3*0)+(2*3)+(1*4)=82
82 % 10 = 2
So 41270-34-2 is a valid CAS Registry Number.

41270-34-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-5-(3-methyl-4-oxo-2-sulfanylidene-1,3-thiazolidin-5-ylidene)-2-sulfanylidene-1,3-thiazolidin-4-one

1.2 Other means of identification

Product number -
Other names Benzene,1,1'-(1E)-1,2-ethenediylbis[3,5-difluoro

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:41270-34-2 SDS

41270-34-2Downstream Products

41270-34-2Relevant articles and documents

Birhodanines and their sulfur analogues for air-stable n-channel organic transistors

Iijima, Kodai,Le Gal, Yann,Higashino, Toshiki,Lorcy, Dominique,Mori, Takehiko

, p. 9121 - 9127 (2017)

A series of thin-film n-channel organic field-effect transistors based on various birhodanines, 3,3′-dialkyl-5,5′-bithiazolidinylidene-2,2′-dione-4,4′-dithiones (OS-R) and their sulfur analogues, 3,3′-dialkyl-5,5′-bithiazolidinylidene-2,4,2′,4′-tetrathiones (SS-R) are studied. The SS-R compounds have tilted stacking crystal structures, whereas the OS-R compounds show basically herringbone structures. The alkyl chain R length and the intermolecular S-S interactions influence the molecular packing to realize excellent long-term air stability in the thin-film transistors.

Studies on fungicides. XXV. Addition reaction of dithiocarbamates to fumaronitrile, bis(alkylthio)maleonitrile, 2,3 dicyano 5,6 dihydro 1,4 dithiin and 4,5 dicyano 2 oxo 1,4 dithiole

Nagase

, p. 505 - 513 (2007/10/05)

-

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 41270-34-2