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406699-89-6

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406699-89-6 Usage

Structure

A quinolinone ring with an acetyl group at the 8th position, a hydroxy group at the 7th position, and a methyl group at the 4th position.

Derivative of quinolinone

Yes

Potential biological activities

Antiviral, antibacterial, and anticancer properties

Potential pharmacological properties

Therapeutic applications in drug development

Need for further research

Yes

Check Digit Verification of cas no

The CAS Registry Mumber 406699-89-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,6,6,9 and 9 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 406699-89:
(8*4)+(7*0)+(6*6)+(5*6)+(4*9)+(3*9)+(2*8)+(1*9)=186
186 % 10 = 6
So 406699-89-6 is a valid CAS Registry Number.

406699-89-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-acetyl-7-hydroxy-4-methylquinolin-2-one

1.2 Other means of identification

Product number -
Other names 2(1H)-Quinolinone, 8-acetyl-7-hydroxy-4-methyl-

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:406699-89-6 SDS

406699-89-6Downstream Products

406699-89-6Relevant articles and documents

Synthesis, photooxygenation, and characterization of new angular furoquinolinone derivatives, a new furocoumarin bioisoster

Elgogary, Sameh,Abd Elghafar, Hoda,Mashaly, Mohammad

, p. 1082 - 1089 (2021/02/01)

Synthesis of angular furoquinolinone derivatives with a new skeleton structure was accomplished via Williamson reaction of hydroxyquinolinones with α-haloketones, such as 3-chloro-2-butanone and phenacyl bromide, followed by treatment with polyphosphoric

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