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35973-27-4

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35973-27-4 Usage

General Description

AURORA 18051 is a chemical compound that is classified as a sesquiterpene lactone. It is a natural product derived from plants and is known for its anti-inflammatory and cytotoxic properties. It has been studied for its potential use in pharmaceuticals for treating various diseases, including cancer and inflammation-related disorders. AURORA 18051 has been shown to exhibit strong bioactivity against cancer cells and is being explored for its potential as a natural alternative for anti-cancer therapy. Additionally, its anti-inflammatory properties make it a promising candidate for the development of new treatments for conditions such as arthritis and inflammatory bowel disease. Overall, AURORA 18051 holds potential for a wide range of therapeutic applications due to its bioactive properties and natural origin.

Check Digit Verification of cas no

The CAS Registry Mumber 35973-27-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,9,7 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 35973-27:
(7*3)+(6*5)+(5*9)+(4*7)+(3*3)+(2*2)+(1*7)=144
144 % 10 = 4
So 35973-27-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H5Cl2NO3/c11-4-1-5-8(7(12)2-4)13-3-6(9(5)14)10(15)16/h1-3H,(H,13,14)(H,15,16)

35973-27-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 6,8-dichloro-4-oxo-1H-quinoline-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 6,8-dichloro-4-hydroxyquinoline-3-carboxylic acid

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:35973-27-4 SDS

35973-27-4Downstream Products

35973-27-4Relevant articles and documents

Dichloro-4-quinolinol-3-carboxylic acid: Synthesis and antioxidant abilities to scavenge radicals and to protect methyl linoleate and DNA

Li, Guo-Xiang,Liu, Zai-Qun,Luo, Xu-Yang

experimental part, p. 1821 - 1827 (2010/06/21)

5,7-, 5,8-, 6,8-, 7,8-Dichloro-4-quinolinol-3-carboxylic acid (5,7-, 5,8-, 6,8-, 7,8-DCQA) together with 7-chloro-4-quinolinol-3-carboxylic acid (7-CQA) and 4-quinolinol-3-carboxylic acid (QA) were synthesized to investigate the antioxidant properties. 5,7-DCQA exhibited the highest ability to scavenge 2,2′-azinobis(3-ethylbenzothiazoline-6-sulfonate) cationic radical (ABTS+.), 2,2′-diphenyl-1-picrylhydrazyl (DPPH) and galvinoxyl radicals. 6,8-DCQA possessed the highest efficacy to protect methyl linoleate against 2,2′-azobis(2-amidinopropane)dihydrochloride (AAPH)-induced oxidation. 5,7-, 5,8-DCQA and QA were able to retard the β-carotene-bleaching in β-carotene-linoleic acid emulsion. In addition, 5,8- and 6,8-DCQA efficiently protected DNA against hydroxyl radical (.OH)-mediated oxidation, and 5,8-DCQA and 7-CQA were active to protect DNA against AAPH-induced oxidation. Furthermore, only 7-CQA can protect DNA against Cu2+/glutathione (GSH)-mediated oxidation. Dichloro-4-quinolinol-3-carboxylic acids were potent to be antiradical drugs, and were worthy to be researched pharmacologically.

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