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2(1H)-Quinolinone, 4-(benzoyloxy)-1-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

685895-32-3

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685895-32-3 Usage

Uses

Chemical research and synthesis, potential pharmaceutical uses

Structure

Quinolinone backbone with a benzoyloxy group attached at the 4th position and a phenyl group attached at the 1st position

Biological activities

Potential applications in medicinal chemistry

Versatility

Diverse potential applications in academic and industrial settings

Check Digit Verification of cas no

The CAS Registry Mumber 685895-32-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,8,5,8,9 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 685895-32:
(8*6)+(7*8)+(6*5)+(5*8)+(4*9)+(3*5)+(2*3)+(1*2)=233
233 % 10 = 3
So 685895-32-3 is a valid CAS Registry Number.

685895-32-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-oxo-1-phenylquinolin-4-yl) benzoate

1.2 Other means of identification

Product number -
Other names HMS1440A12

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:685895-32-3 SDS

685895-32-3Relevant academic research and scientific papers

Ring closure reactions of 3-arylhydrazonoalkyl-quinolin-2-ones to 1-aryl-pyrazolo[4,3-c]quinolin-2-ones

Stadlbauer, Wolfgang,Hojas, Gerhard

, p. 681 - 690 (2007/10/03)

4-Hydroxy-3-arylhydrazonoalkyl-2-quinolones 6 or reactive derivatives such as 3-arylhydrazonoalkyl-4-tosyloxy-2-quinolones 7 or 4-chloro-3- arylhydrazonoalkyl-2-quinolones 14, which are obtained via 3-acyl-4- hydroxyquinolones 4, 10 or 3-phenylaminomethylene-quinoline-2,4-diones 12, cyclize in excellent yields to 1-aryl-pyrazolo[4,3-c]quinolin-4-ones (11). The cyclization conditions were investigated by differential scanning calorimetry (DSC).

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