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Decanoic acid, 10-oxo-10-(phenylamino)-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

64785-83-7

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64785-83-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64785-83-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,7,8 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 64785-83:
(7*6)+(6*4)+(5*7)+(4*8)+(3*5)+(2*8)+(1*3)=167
167 % 10 = 7
So 64785-83-7 is a valid CAS Registry Number.

64785-83-7SDS

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 9-phenylcarbamoyl-nonanoic acid methyl ester

1.2 Other means of identification

Product number -
Other names 9-Phenylcarbamoyl-nonansaeure-methylester

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:64785-83-7 SDS

64785-83-7Relevant academic research and scientific papers

A natural product inspired fragment-based approach towards the development of novel anti-bacterial agents

Austin, Michael J.,Hearnshaw, Stephen J.,Mitchenall, Lesley A.,McDermott, Paul J.,Howell, Lesley A.,Maxwell, Anthony,Searcey, Mark

, p. 1387 - 1391 (2016)

The discovery of new antibiotics with novel modes of action to combat antimicrobial resistance (AMR) is of vital importance. The natural product simocyclinone D8 (SD8) is a potent inhibitor of DNA gyrase. Its bi-functional structure and novel mode of action serve as an inspiring lead for antibiotic development. Herein we describe a proof of principle fragment-based approach towards the development of a new class of coumarin-quinolone hybrids. We demonstrate that the coumarin moiety is required for the observed inhibitory activity (IC50 ~ 3 μM) of the hybrid compound, which is in part mediated through stabilisation of a cleaved-DNA intermediate.

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