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4-(benzylamino)-3-nitro-2H-chromen-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

50527-29-2

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50527-29-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50527-29-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,5,2 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 50527-29:
(7*5)+(6*0)+(5*5)+(4*2)+(3*7)+(2*2)+(1*9)=102
102 % 10 = 2
So 50527-29-2 is a valid CAS Registry Number.

50527-29-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(benzylamino)-3-nitrochromen-2-one

1.2 Other means of identification

Product number -
Other names 4-Benzylamino-3-nitro-chromen-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:50527-29-2 SDS

50527-29-2Relevant academic research and scientific papers

A small library of 4-(alkylamino)-3-nitrocoumarin derivatives with potent antimicrobial activity against gastrointestinal pathogens

Radulovi?, Niko S.,Stojanovi?-Radi?, Zorica,Stojanovi?, Predrag,Stojanovi?, Nikola,Deki?, Vidoslav,Deki?, Biljana

, p. 315 - 327 (2015/06/16)

Due to the confirmed antimicrobial activity of both natural and synthetic coumarin derivatives, the present study was envisaged to provide further insight into the antimicrobial potential of coumarins through the screening of a designed library of nine 4-(alkylamino)-3-nitrocoumarins against a panel of 24 laboratory strains and resistant (isolates) bacterial and fungal pathogens. All compounds showed some degree of strain-selective activity that in some cases was very pronounced, reaching the value of 0.04 nmol mL-1 (i.e., 12 ng mL-1) for the minimal inhibitory concentration against Candida albicans. The observed activities were higher against Gram-negative strains, among which the most susceptible strain, among both ATCC strains and clinical isolates, was Salmonella enterica subsp. enterica serovar Enteritidis. These results indicate to a high potential of these coumarins as antimicrobials for the treatment of gastrointestinal and other infections caused by highly resistant microbial strains. Finally, a multivariate statistical analysis of the herein obtained and previous results on the antimicrobial activity of related selected coumarins was performed to allow an easier structure-activity discussion.

A small library of 4-(alkylamino)-3-nitrocoumarin derivatives with potent antimicrobial activity against gastrointestinal pathogens

Radulovi, Niko S.,Stojanovi-Radi, Zorica,Stojanovi, Predrag,Stojanovi, Nikola,Deki, Vidoslav,Deki, Biljana

, (2015/03/03)

Abstract: Due to a confirmed antimicrobial activity of both natural and synthetic coumarin derivatives, the present study was envisaged to provide a further insight into the antimicrobial potential of coumarins through a screening of a designed library of nine 4-(alkylamino)-3-nitrocoumarins against a panel of 24 laboratory strains and resistant (isolates) bacterial and fungal pathogens. All compounds showed some degree of strain-selective activity, that was, in some cases, very pronounced, reaching the value of 0.04 nmol/ml (i.e. 12 ng/ml) for the minimal inhibitory concentration against Candida albicans. The observed activity was higher against Gram-negative strains, among which the most susceptible strain, among both ATCC strains and clinical isolates, was Salmonella enteritidis. These results point out to a high potential of these coumarins as antimicrobials for the treatment of gastrointestinal and other infections caused by highly resistant microbial strains. Finally, a multivariate statistical analysis of the herein obtained and previous results on the antimicrobial activity of related selected coumarins was performed to allow an easier structure-activity discussion.

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