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31404-08-7

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31404-08-7 Usage

General Description

2-(4-Methoxy-phenyl)-Thiazolidine is a chemical compound that falls under the category of organic compounds, specifically thiazolidines. Known also by its IUPAC name 2-(4-methoxyphenyl)-1,3-thiazolidine, this compound is structured with a thiazolidine backbone connected to a 4-methoxyphenyl group. The thiazolidine ring is a five-membered heterocyclic compound featuring sulfur and nitrogen atoms, while the 4-methoxyphenyl group is a phenyl ring attached to a methoxy group. 2-(4-METHOXY-PHENYL)-THIAZOLIDINE can be utilized in the synthesis of various pharmaceuticals or as a building block in organic chemistry, though specific details about its uses are not widely documented in public databases. Further studies are needed to better understand its properties and potential applications.

Check Digit Verification of cas no

The CAS Registry Mumber 31404-08-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,4,0 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 31404-08:
(7*3)+(6*1)+(5*4)+(4*0)+(3*4)+(2*0)+(1*8)=67
67 % 10 = 7
So 31404-08-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H13NOS/c1-12-9-4-2-8(3-5-9)10-11-6-7-13-10/h2-5,10-11H,6-7H2,1H3

31404-08-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-methoxyphenyl)-1,3-thiazolidine

1.2 Other means of identification

Product number -
Other names F0804-1064

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:31404-08-7 SDS

31404-08-7Relevant articles and documents

First example of the ring-opening transformation of thiazolidines to iminothiols on gold surface

Majouga, Alexander G.,Beloglazkina, Elena K.,Yudin, Ivan V.,Rakhimov, Rustem D.,Khlobystov, Andrei N.,Zyk, Nikolai V.

, p. 92 - 93 (2009)

A new way to construction of the self-assembling monolayers on gold surfaces based on ring opening reactions of thiazolidines to iminothiols followed by Au-S bond formation has been proposed.

Evolution of thiazolidine-based blockers of human Kv1.5 for the treatment of atrial arrhythmias

Jackson, Chris M.,Blass, Benjamin,Coburn, Keith,Djandjighian, Laurent,Fadayel, Gina,Fluxe, Andrew J.,Hodson, Steven J.,Janusz, John M.,Murawsky, Michael,Ridgeway, James M.,White, Ronald E.,Wu, Shengde

, p. 282 - 284 (2007/10/03)

Blockade of the Kv1.5 ion channel is a potentially atrial-selective avenue for the treatment of atrial fibrillation and atrial flutter. The development and biological evaluation of a series of thiazolidine-based blockers of Kv1.5 is described.

Synthesis of 2-phenylthiazolidine derivatives as cardiotonic agents. I. 2-Phenylthiazolidine-3-thiocarboxamides.

Nate,Sekine,Honma,Nakai,Wada,Takeda,Yabana,Nagao

, p. 1953 - 1968 (2007/10/02)

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