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42414-28-8

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42414-28-8 Usage

General Description

4,6,8-trimethyl-quinolin-2-ol is a chemical compound with the molecular formula C13H13NO. It is an organic compound that belongs to the class of quinoline derivatives. 4,6,8-TRIMETHYL-QUINOLIN-2-OL is a derivative of quinolinol, with three methyl groups attached to the 4th, 6th, and 8th carbon atoms of the quinoline ring. It is often used as a building block in the synthesis of various organic compounds and is also of interest in medical and pharmaceutical research due to its potential biological activities. The exact properties and uses of 4,6,8-trimethyl-quinolin-2-ol may vary depending on its specific application and the context in which it is used.

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 articles and documents

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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