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4,6,8-TRIMETHYL-QUINOLIN-2-OL, with the molecular formula C13H13NO, is an organic compound belonging to the class of quinoline derivatives. It is a derivative of quinolinol, characterized by the presence of three methyl groups attached to the 4th, 6th, and 8th carbon atoms of the quinoline ring. 4,6,8-TRIMETHYL-QUINOLIN-2-OL is frequently utilized as a building block in the synthesis of various organic compounds and holds potential for biological activities, making it a subject of interest in medical and pharmaceutical research.

42414-28-8

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42414-28-8 Usage

Uses

Used in Organic Synthesis:
4,6,8-TRIMETHYL-QUINOLIN-2-OL is used as a building block for the synthesis of various organic compounds, contributing to the development of new chemical entities with diverse applications.
Used in Medical and Pharmaceutical Research:
In the field of medical and pharmaceutical research, 4,6,8-TRIMETHYL-QUINOLIN-2-OL is used as a compound of interest due to its potential biological activities, which may lead to the discovery of new therapeutic agents or contribute to understanding complex biological processes.

Check Digit Verification of cas no

The CAS Registry Mumber 42414-28-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,4,1 and 4 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 42414-28:
(7*4)+(6*2)+(5*4)+(4*1)+(3*4)+(2*2)+(1*8)=88
88 % 10 = 8
So 42414-28-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H13NO/c1-7-4-9(3)12-10(5-7)8(2)6-11(14)13-12/h4-6H,1-3H3,(H,13,14)

42414-28-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,6,8-trimethyl-1H-quinolin-2-one

1.2 Other means of identification

Product number -
Other names F3284-7635

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:42414-28-8 SDS

42414-28-8Relevant academic research and scientific papers

Synthesis of 2-Quinolinones via a Hypervalent Iodine(III)-Mediated Intramolecular Decarboxylative Heck-Type Reaction at Room Temperature

Fan, Huaqiang,Pan, Peng,Zhang, Yongqiang,Wang, Wei

, p. 7929 - 7932 (2019/01/04)

A hypervalent iodine(III)-mediated intramolecular decarboxylative Heck-type reaction of 2-vinyl-phenyl oxamic acids has been developed. The unique ring-strain-enabled radical decarboxylation mechanism is preliminarily revealed. This protocol features metal-free reaction conditions and operational simplicity, allowing the lactamization of 2-vinylanilines using a readily accessible carbonyl source and the synthesis of various 2-quinolinones with excellent chemoselectivity at room temperature.

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