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59387-82-5

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59387-82-5 Usage

Molecular weight

237.28 g/mol

Classification

quinolinium derivative

Structure

contains a quinoline ring with an amino group and a carbonyl group attached; phenyl group attached to the quinolinium ring

Applications

used in medicinal chemistry and pharmaceutical research for potential anti-cancer and anti-inflammatory properties, as well as a fluorescent probe for the detection of metal ions.

Check Digit Verification of cas no

The CAS Registry Mumber 59387-82-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,3,8 and 7 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 59387-82:
(7*5)+(6*9)+(5*3)+(4*8)+(3*7)+(2*8)+(1*2)=175
175 % 10 = 5
So 59387-82-5 is a valid CAS Registry Number.

59387-82-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-hydroxy-3-phenylquinolin-2-imine

1.2 Other means of identification

Product number -
Other names 2-amino-3-phenylquinolin-1-ol

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:59387-82-5 SDS

59387-82-5Downstream Products

59387-82-5Relevant articles and documents

Novel and efficient synthesis of substituted quinoline-1-oxides and the complex compounds SnL2Cl2 (L=2-aminoquinoline-1-oxides) with the aid of stannous chloride

Fu, Lei,Lin, Wei,Xu, Pan,Xi, Yu-Kun,Wang, Man-Man,Shi, Da-Qing

experimental part, p. 7782 - 7786 (2012/09/22)

A novel and efficient approach to the synthesis of substituted quinoline-1-oxides and the complex compounds SnL2Cl2 (L=2-aminoquinoline-1-oxides) was developed. The reaction has fancy selectivity when 3-(2-nitrophenyl)acrylonitriles were treated with the aid of SnCl 2 reagent under the same conditions. When R is -CN or -COOR′ the complex compounds SnL2Cl2 (L=2-aminoquinoline-1- oxides) were obtained. Whereas, when R is H or aryl another series of substituted quinoline-1-oxides were formed. The products have been screened for their anticancer activities.

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