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Hydrazinecarbothioamide, 2-[(2-chloro-8-methyl-3-quinolinyl)methylene]-N-cyclohexyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

104827-61-4

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104827-61-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104827-61-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,8,2 and 7 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 104827-61:
(8*1)+(7*0)+(6*4)+(5*8)+(4*2)+(3*7)+(2*6)+(1*1)=114
114 % 10 = 4
So 104827-61-4 is a valid CAS Registry Number.

104827-61-4SDS

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 1-((2-chloro-8-methylquinolin-3-yl)methylene)-4-cyclohexylthiosemicarbazide

1.2 Other means of identification

Product number -
Other names -

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:104827-61-4 SDS

104827-61-4Relevant articles and documents

3-(1,3,4-Thiadiazole-2-yl)quinoline derivatives: Synthesis, characterization and anti-microbial activity

Bhat, Abdul R.,Tazeem,Azam, Amir,Choi, Inho,Athar, Fareeda

, p. 3158 - 3166 (2011/06/26)

A new series of thiadiazoles and intermediate thiosemicarbazones were synthesized from the chloroquinone molecule, with an aim to explore their effect on in vitro growth of microorganisms causing microbial infection. The chemical structures of the compound were elucidated by elemental analysis, FTIR, 1H and 13C NMR and ESI-MS spectral data. In vitro anti-microbial activity was performed against Staphylococcusaureus, Streptococcuspyogenes, Salmonellatyphimurium, and Escherichiacoli. The MIC was detected using the double dilution method. The results were compared by calculating percent inhibit area/μg of the compounds and the standard "amoxicillin". The selected compounds were tested for cytotoxic results using MTT assay H9c2 cardiac myoblasts cell line and the results showed that all the compounds offered remarkable >80% viability to a concentration of 200 μg/mL.

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