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8-Methoxy-1-methyl-1H-quinolin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60443-14-3

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60443-14-3 Usage

Synthesis Reference(s)

Synthetic Communications, 19, p. 3523, 1989 DOI: 10.1080/00397918908052761

Check Digit Verification of cas no

The CAS Registry Mumber 60443-14-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,4,4 and 3 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 60443-14:
(7*6)+(6*0)+(5*4)+(4*4)+(3*3)+(2*1)+(1*4)=93
93 % 10 = 3
So 60443-14-3 is a valid CAS Registry Number.

60443-14-3SDS

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 8-methoxy-1-methylquinolin-2-one

1.2 Other means of identification

Product number -
Other names 1-methyl-8-(methyloxy)-2(1H)-quinolinone

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:60443-14-3 SDS

60443-14-3Downstream Products

60443-14-3Relevant academic research and scientific papers

An organocatalyst bound α-aminoalkyl radical intermediate for controlled aerobic oxidation of iminium ions

Motaleb, Abdul,Bera, Asish,Maity, Pradip

, p. 5081 - 5085 (2018/07/29)

A catalyst bound α-aminoalkyl radical intermediate from iminium is developed to control its formation and reactivity with aerobic oxygen. The influence of the catalyst was demonstrated via the ease of radical intermediate formation and its subsequent reactivity, including the first catalyst-controlled enantioselective aerobic oxidation with a chiral phosphite catalyst.

SUBSTITUTED 1-METHYL-1H-QUINOLIN-2-ONES AND 1-METHYL-1H-1,5-NAPHTHYRIDIN-2-ONES AS ANTIBACTERIALS

-

Page/Page column 42-43, (2008/06/13)

Bicyclic nitrogen containing compounds of formula (I) and their use as antibacterials.

Synthesis of methoxy-2-quinolones via Pummerer-type cyclization of N-aryl-N-methyl-3-(phenylsulfinyl)propionamides

Toda,Sakagami,Goan,Simakata,Saitoh,Horiguchi,Sano

, p. 1854 - 1861 (2007/10/03)

The thionium ions 10 generated by Pummerer reaction of N-aryl-N-methyl-3-(phenylsulfinyl)propionamides 4 caused not only an electrophilic cyclization reaction producing 2-quinolones 8, but also the formation of the vinyl sulfides 5 and 6 in favor of the l

AN EFFICIENT SYNTHESIS OF 8-METHOXY- AND 8-HYDROXY-1-METHYLCARBOSTYRIL.

Gesto, C.,Cuesta, E. de la,Avendano, C.

, p. 35 - 39 (2007/10/02)

An efficient procedure to obtain 8-methoxy-1-methylcarbostyril from 8-hydroxyquinoline through 8-methoxyquinoline methiodide is described.

AN EFFICIENT SYNTHESIS OF 8-METHOXY- AND 8-HYDROXY-1-METHYLCARBOSTYRIL

Gesto, C.,Cuesta, E. de la,Avedano, C.

, p. 3523 - 3528 (2007/10/02)

An efficient procedure to obtain 8-methoxy-1-methylcarbostyril from 8-hydroxyquinoline through 8-methoxyquinoline methiodide is described.

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