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20240-21-5

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20240-21-5 Usage

General Description

4-Thiazolecarboxylic acid,4,5-dihydro-2-(6-hydroxy-2-benzothiazolyl)- is a chemical compound with a complex structure consisting of a thiazole ring and a benzothiazole ring. It is categorized as a carboxylic acid due to the presence of a carboxyl group in its structure. Its molecular formula is C12H9N3O3S2, showing that it contains carbon, hydrogen, nitrogen, oxygen, and sulfur atoms. 4-Thiazolecarboxylic acid,4,5-dihydro-2-(6-hydroxy-2-benzothiazolyl)- has potential pharmacological and biological activities due to the presence of two heterocyclic rings and a hydroxy group, making it an interesting molecule for further research in the fields of medicinal chemistry and drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 20240-21-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,2,4 and 0 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 20240-21:
(7*2)+(6*0)+(5*2)+(4*4)+(3*0)+(2*2)+(1*1)=45
45 % 10 = 5
So 20240-21-5 is a valid CAS Registry Number.

20240-21-5SDS

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 2-(6-Hydroxy-1,3-benzothiazol-2-yl)-4,5-dihydro-1,3-thiazole-4-ca rboxylic acid

1.2 Other means of identification

Product number -
Other names 2-thien-2-yl-4,5-dihydro-1H-imidazole

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:20240-21-5 SDS

20240-21-5Relevant articles and documents

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White,E.H. et al.

, p. 2344 - 2348 (1965)

-

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White et al.

, (1963)

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On the use of peroxy-caged luciferin (PCL-1) probe for bioluminescent detection of inflammatory oxidants in vitro and in vivo – Identification of reaction intermediates and oxidant-specific minor products

Zielonka, Jacek,Podsiad?y, Rados?aw,Zielonka, Monika,Hardy, Micael,Kalyanaraman, Balaraman

, p. 32 - 42 (2016/08/04)

Peroxy-caged luciferin (PCL-1) probe was first used to image hydrogen peroxide in living systems (Van de Bittner et al., 2010 [9]). Recently this probe was shown to react with peroxynitrite more potently than with hydrogen peroxide (Sieracki et al., 2013 [11]) and was suggested to be a more suitable probe for detecting peroxynitrite under in vivo conditions. In this work, we investigated in detail the products formed from the reaction between PCL-1 and hydrogen peroxide, hypochlorite, and peroxynitrite. HPLC analysis showed that hydrogen peroxide reacts slowly with PCL-1, forming luciferin as the only product. Hypochlorite reaction with PCL-1 yielded significantly less luciferin, as hypochlorite oxidized luciferin to form a chlorinated luciferin. Reaction between PCL-1 and peroxynitrite consists of a major and minor pathway. The major pathway results in luciferin and the minor pathway produces a radical-mediated nitrated luciferin. Radical intermediate was characterized by spin trapping. We conclude that monitoring of chlorinated and nitrated products in addition to bioluminescence in vivo will help identify the nature of oxidant responsible for bioluminescence derived from PCL-1.

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