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172604-63-6

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172604-63-6 Usage

Quinolinone class

This compound belongs to the quinolinone class of compounds, which are known for their chemical and biological activity.

Hydroxyl and methyl groups

The compound contains a hydroxyl (-OH) and a methyl (-CH3) group, which can affect its reactivity and physical properties.

Pharmaceutical and agrochemical synthesis

2(1H)-Quinolinone,3-hydroxy-1-methyl-(9CI) is used in the synthesis of pharmaceuticals and agrochemicals, indicating its potential for practical applications.

Organic synthesis and medicinal chemistry

The compound may have potential applications in the field of organic synthesis and medicinal chemistry, suggesting that it could be used to develop new compounds for various purposes.

Valuable building block

The specific properties and reactivity of 2(1H)-Quinolinone,3-hydroxy-1-methyl-(9CI) make it a valuable building block in the development of new compounds for various industrial and research purposes.

Check Digit Verification of cas no

The CAS Registry Mumber 172604-63-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,2,6,0 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 172604-63:
(8*1)+(7*7)+(6*2)+(5*6)+(4*0)+(3*4)+(2*6)+(1*3)=126
126 % 10 = 6
So 172604-63-6 is a valid CAS Registry Number.

172604-63-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-hydroxy-1-methylquinolin-2(1H)-one

1.2 Other means of identification

Product number -
Other names 3-hydroxy-1-methyl-1H-quinolin-2-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:172604-63-6 SDS

172604-63-6Relevant articles and documents

Pinacol rearrangement of 3,4-dihydro-3,4-dihydroxyquinolin-2(1H)-ones: An alternative pathway to viridicatin alkaloids and their analogs

Rudolf, Ondrej,Rouchal, Michal,Lycka, Antonin,Klasek, Antonin

, p. 1905 - 1917 (2013/11/06)

3-Alkyl/aryl-3-hydroxyquinoline-2,4-diones were reduced with NaBH 4 to give cis-3-alkyl/aryl-3,4-dihydro-3,4-dihydroxyquinolin-2(1H)- ones. These compounds were subjected to pinacol rearrangement by treatment with concentrated H2SOs

NITROGEN-CONTAINING COMPOUND AND PHARMACEUTICAL COMPOSITION

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Page/Page column 421, (2011/04/13)

The present invention provides a novel diazepine compound that blocks the IKur current or the Kv1.5 channel potently and more selectively than other K+ channels. The present invention relates to a diazepine compound represented by General Formula (1) or a salt thereof, wherein R1, R2, R3, and R4 are each independently hydrogen, lower alkyl, cyclo lower alkyl or lower alkoxy lower alkyl; R2 and R3 may be linked to form lower alkylene; A1 is lower alkylene optionally substituted with one or more substituents selected from the group consisting of hydroxyl and oxo; Y1 and Y2 are each independently -N= or -CH=; and R5 is group represented by (2) wherein R6 and R7 are each independently hydrogen or organic group; R6 and R7 may be linked to form a ring together with the neighboring group -XA-N-XB-; XA and XB are each independently a bond, lower alkylene, etc.

Reactions of Diazo Compounds with Isatin and its Derivatives

Kennewell, Peter D.,Miller, David J.,Scrowston, Richard M.,Westwood, Robert

, p. 2380 - 2388 (2007/10/03)

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