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100717-76-8

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100717-76-8 Usage

General Description

3-butyl-2-hydroxy-1-methylquinolin-4(1H)-one, also known as ethyl hydrogen 6-keto-2-methyl-4-hydroxyquinoline-3-carboxylate or Coenzyme Q3, is a chemical compound with antioxidant properties. It is a derivative of Coenzyme Q, a vital component in the electron transport chain for cellular respiration. 3-butyl-2-hydroxy-1-methylquinolin-4(1H)-one has been studied for its potential use in treating diseases related to mitochondrial dysfunction, such as cardiovascular disease and neurodegenerative disorders. It has also shown promising results in protecting cells from oxidative stress and preventing damage caused by free radicals. Additionally, Coenzyme Q3 has demonstrated potential for use in cosmetic formulations due to its antioxidant and anti-aging properties.

Check Digit Verification of cas no

The CAS Registry Mumber 100717-76-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,7,1 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 100717-76:
(8*1)+(7*0)+(6*0)+(5*7)+(4*1)+(3*7)+(2*7)+(1*6)=88
88 % 10 = 8
So 100717-76-8 is a valid CAS Registry Number.

100717-76-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-butyl-4-hydroxy-1-methylquinoline-2(1H)-one

1.2 Other means of identification

Product number -
Other names 3-Butyl-4-hydroxy-1-methylquinolin-2(1H)-one

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:100717-76-8 SDS

100717-76-8Relevant articles and documents

A simple and effective method for the reduction of acyl substituted heterocyclic 1,3-dicarbonyl compounds to alkyl derivatives by zinc - acetic acid - hydrochloric acid

Kappe, Thomas,Aigner, Rudolf,Roschger, Peter,Schnell, Barbara,Stadlbauer, Wolfgang

, p. 12923 - 12928 (1995)

3-Acyl-4-hydroxy-2(1H)-quinolones (1a-k) were reduced in good yields (66-97%) to 3-alkyl-4-hydroxy-2(1H)-quinolinones (2a-k) using zinc powder (particle size 〈45 μm) in acetic acid/hydrochloric acid. This method could be transformed to 3-acetyl-4-hydroxy-

Reaction of Tertiary 2-Chloroketones with Cyanide Ions: Application to 3-Chloroquinolinediones

Bedná?, Luká?,Kafka, Stanislav,Klásek, Antonín,Ly?ka, Antonín,Rouchal, Michal,Rudolf, Ond?ej

, p. 645 - 652 (2021/07/22)

3-Chloroquinoline-2,4-diones react with cyanide ions in dimethyl formamide to give 3-cyanoquinoline-2,4-diones in small yields due to the strong hindrance of the substituent at the C-3 atom. Good yields can be achieved if the substituent at this position

Oxidative ring opening of 3-hydroxyquinoline-2,4(1H,3H)-diones into N-(α-ketoacyl)anthranilic acids Dedicated to Professor Slovenko Polanc on his 65th birthday

Kafka, Stanislav,Proisl, Karel,Ka?párková, Věra,Urankar, Damijana,Kimmel, Roman,Ko?mrlj, Janez

, p. 10826 - 10835 (2014/01/06)

N-(α-Ketoacyl)anthranilic acids were prepared by oxidative ring opening of 3-hydroxyquinoline-2,4(1H,3H)-diones by using paraperiodic acid (H5IO6) or sodium periodate (NaIO4). The optimisation of the reaction conditions is

Reaction of 3-hydroxyquinoline-2,4-diones with isocyanates and thermally induced transformation of the reaction products

Mrkvicka, Vladimir,Lycka, Antonin,Vicha, Robert,Klasek, Antonin

experimental part, p. 78 - 91 (2011/03/16)

3-Hydroxyquinoline-2,4-diones 1 react with isocyanates to give novel 1,2,3,4-tetrahydro-2,4-dioxoquinolin-3-yl (alkyl/aryl)carbamates 2 and/or 1,9b-dihydro-9b-hydroxyoxazolo[5,4-c]quinoline-2,4(3aH,5H)-diones 3. Both of these compounds are converted, by boiling in cyclohexylbenzene solution in the presence of Ph3P or 4-(dimethylamino)pyridine, to give 3-(acyloxy)-1,3-dihydro-2H-indol-2-ones 8. All compounds were characterized by IR, and 1H- and 13C-NMR spectroscopy, as well as by EI mass spectrometry. Copyright

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