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23176-01-4

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23176-01-4 Usage

General Description

3-Thiazolidineacetic acid, 4-oxo-2-thioxo-, ethyl ester is a compound with the molecular formula C7H9NO3S. It is the ethyl ester of 3-thiazolidineacetic acid, which is a derivative of acetic acid. This chemical is used in various pharmaceutical and chemical applications, including as a building block for the synthesis of other organic compounds. It is known for its ability to act as a strong antioxidant, as well as its potential anti-inflammatory and antimicrobial properties. Additionally, research has shown that this compound may have potential therapeutic effects in the treatment of various diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 23176-01-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,1,7 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 23176-01:
(7*2)+(6*3)+(5*1)+(4*7)+(3*6)+(2*0)+(1*1)=84
84 % 10 = 4
So 23176-01-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H9NO3S2/c1-2-11-6(10)3-8-5(9)4-13-7(8)12/h2-4H2,1H3

23176-01-4SDS

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 ethyl 2-(4-oxo-2-sulfanylidene-1,3-thiazolidin-3-yl)acetate

1.2 Other means of identification

Product number -
Other names 3-Rhodanineacetic acid,ethyl ester

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:23176-01-4 SDS

23176-01-4Relevant articles and documents

Synthesis and structure-activity relationship studies of 2,4-thiazolidinediones and analogous heterocycles as inhibitors of dihydrodipicolinate synthase

Christoff, Rebecca M.,Soares da Costa, Tatiana P.,Bayat, Saadi,Holien, Jessica K.,Perugini, Matthew A.,Abbott, Belinda M.

supporting information, (2021/11/27)

Dihydrodipicolinate synthase (DHDPS), responsible for the first committed step of the diaminopimelate pathway for lysine biosynthesis, has become an attractive target for the development of new antibacterial and herbicidal agents. Herein, we report the di

HETEROCYCLIC INHIBITORS OF LYSINE BIOSYNTHESIS VIA THE DIAMINOPIMELATE PATHWAY

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Paragraph 0195, (2018/11/10)

The present invention relates to certain heterocyclic compounds of formula (1) that have the ability to inhibit lysine biosynthesis via the diaminopimelate biosynthesis pathway in certain organisms. As a result of this activity these compounds can be used

Novel phenothiazine derivative and preparation method and application thereof

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Paragraph 0063; 0064; 0065, (2017/01/02)

The invention discloses a novel phenothiazine derivative and a preparation method and application thereof, and belongs to the technical field of biological medicines. The invention particularly discloses a compound of a structural general formula I and salts, applicable in pharmacy, of the compound, and the compound and the salts can be used as near-infrared fluorescent molecular probes. The invention further provides a preparation method of the molecular probes and application of the molecular probes. Fluorescent molecules are novel in structure, good in sensitivity and selectivity and good in light stability. The molecules and Abeta(1-42) aggregates have good affinity, and meanwhile auto-polymerization of beta-amyloid protein can be well inhibited. Therefore, the probes can be applied to imaging of Abeta amyloid plaque and can be used for treating the Alzheimer's disease.

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