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2-Chloro-4-methyl-5-nitroquinoline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

54965-60-5

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54965-60-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54965-60-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,9,6 and 5 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 54965-60:
(7*5)+(6*4)+(5*9)+(4*6)+(3*5)+(2*6)+(1*0)=155
155 % 10 = 5
So 54965-60-5 is a valid CAS Registry Number.

54965-60-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-4-methyl-5-nitroquinoline

1.2 Other means of identification

Product number -
Other names 2-chloro-4-methyl-5-nitro-quinoline

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:54965-60-5 SDS

54965-60-5Upstream product

54965-60-5Relevant academic research and scientific papers

Pyridoquinolones containing azetidinones: Synthesis and their biological evaluation

Patel, Navin B.,Pathak, Kunal K.

, p. 2044 - 2055,12 (2012)

A series of pyridoquinolone 4-oxo-1,4-dihydro( 40-methyl-60-chloropyrido[2, 3-h])quinoline-3-[N-(substituted phenyl methylidine)]carbohydrazide 3a-j and 4-oxo-1, 4-dihydro(4′-methyl-6′-chloropyrido[2,3-h])-3-[N-{(3- chloro- 2-oxo-4-(substituted phenyl) azetidine-1-yl)amino}carbonyl] quinoline 4a-j have been synthesized via 4-oxo-1, 4-dihydro-(4′-methyl-6′- chloropyrido[2,3-h])quinoline carboxylate 1. All the compounds were proved by IR, 1H-NMR, 13C-NMR spectral studies and elemental analysis. Antibacterial activities (MIC) against E. coli, P. aeruginosa, S. aureus and S. pyogenes, and antifungal activities against C. albicans, A. niger and A. clavatus were screened, whereas selected compounds were screened against Mycobacterium tuberculosis H37Rv and compared with standard drugs.

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