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ethyl 2-chloro-6-nitroquinoline-4-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55878-86-9

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55878-86-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55878-86-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,8,7 and 8 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 55878-86:
(7*5)+(6*5)+(5*8)+(4*7)+(3*8)+(2*8)+(1*6)=179
179 % 10 = 9
So 55878-86-9 is a valid CAS Registry Number.

55878-86-9SDS

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 ethyl 2-chloro-6-nitroquinoline-4-carboxylate

1.2 Other means of identification

Product number -
Other names 4-Quinolinecarboxylic acid,2-chloro-6-nitro-,ethyl ester

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:55878-86-9 SDS

55878-86-9Downstream Products

55878-86-9Relevant academic research and scientific papers

Construction and functionalization of fused pyridine ring leading to novel compounds as potential antitubercular agents

Dulla, Balakrishna,Wan, Baojie,Franzblau, Scott G.,Kapavarapu, Ravikumar,Reiser, Oliver,Iqbal, Javed,Pal, Manojit

supporting information; experimental part, p. 4629 - 4635 (2012/07/31)

A series of fused and functionalized pyridine derivatives were designed, synthesized and tested for their potential antitubercular properties. All these novel compounds were prepared by using multistep methods involving the construction of pyridine ring as a key synthetic step. Some of these compounds were found to be interesting when tested for their antitubercular properties in vitro and one of them appeared as an attractive and potential antitubercular agent.

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