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1,4-Benzenedicarboxamide,N1,N4-bis[4-(4,5-dihydro-1H-imidazol-2-yl)phenyl]-2-nitro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

14599-52-1

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14599-52-1 Usage

Composition

Benzenedicarboxamide backbone with two nitro groups and two 4-(4,5-dihydro-1H-imidazol-2-yl)phenyl substituents

Physical State

Crystalline solid at room temperature

Application

Used in the manufacturing of polymers, specifically polyimides

Properties

High thermal stability and mechanical strength

Additional Uses

Intermediate in the synthesis of pharmaceuticals and other fine chemicals

Potential Industries

Plastics, pharmaceuticals, and materials science

Check Digit Verification of cas no

The CAS Registry Mumber 14599-52-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,5,9 and 9 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 14599-52:
(7*1)+(6*4)+(5*5)+(4*9)+(3*9)+(2*5)+(1*2)=131
131 % 10 = 1
So 14599-52-1 is a valid CAS Registry Number.

14599-52-1SDS

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 1-N,4-N-bis[4-(4,5-dihydro-1H-imidazol-2-yl)phenyl]-2-nitrobenzene-1,4-dicarboxamide

1.2 Other means of identification

Product number -
Other names n,n'-bis[4-(4,5-dihydro-1h-imidazol-2-yl)phenyl]-2-nitrobenzene-1,4-dicarboxamide

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:14599-52-1 SDS

14599-52-1Downstream Products

14599-52-1Relevant academic research and scientific papers

Identification and Structure-Activity Relationships of Novel Compounds that Potentiate the Activities of Antibiotics in Escherichia coli

Haynes, Keith M.,Abdali, Narges,Jhawar, Varsha,Zgurskaya, Helen I.,Parks, Jerry M.,Green, Adam T.,Baudry, Jerome,Rybenkov, Valentin V.,Smith, Jeremy C.,Walker, John K.

, p. 6205 - 6219 (2017)

In Gram-negative bacteria, efflux pumps are able to prevent effective cellular concentrations from being achieved for a number of antibiotics. Small molecule adjuvants that act as efflux pump inhibitors (EPIs) have the potential to reinvigorate existing antibiotics that are currently ineffective due to efflux mechanisms. Through a combination of rigorous experimental screening and in silico virtual screening, we recently identified novel classes of EPIs that interact with the membrane fusion protein AcrA, a critical component of the AcrAB-TolC efflux pump in Escherichia coli. Herein, we present initial optimization efforts and structure-activity relationships around one of those previously described hits, NSC 60339 (1). From these efforts we identified two compounds, SLUPP-225 (17h) and SLUPP-417 (17o), which demonstrate favorable properties as potential EPIs in E. coli cells including the ability to penetrate the outer membrane, improved inhibition of efflux relative to 1, and potentiation of the activity of novobiocin and erythromycin.

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