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4-[(E)-(4-chlorophenyl)diazenyl]-3,5-dimethyl-1H-pyrazole-1-carbothioamide is a complex organic compound with the molecular formula C13H12ClN5S. It is characterized by a pyrazole ring, which is substituted with a 4-chlorophenyl diazenyl group at the 4-position and a carbothioamide group at the 1-position. The molecule also features two methyl groups at the 3 and 5 positions of the pyrazole ring. 4-[(E)-(4-chlorophenyl)diazenyl]-3,5-dimethyl-1H-pyrazole-1-carbothioamide is known for its potential applications in pharmaceutical research, particularly as an intermediate in the synthesis of various drugs. Its chemical structure and properties make it a subject of interest for scientists exploring new therapeutic agents.

1867-30-7

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1867-30-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1867-30-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,6 and 7 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1867-30:
(6*1)+(5*8)+(4*6)+(3*7)+(2*3)+(1*0)=97
97 % 10 = 7
So 1867-30-7 is a valid CAS Registry Number.

1867-30-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[(4-chlorophenyl)diazenyl]-3,5-dimethylpyrazole-1-carbothioamide

1.2 Other means of identification

Product number -
Other names F 2358

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:1867-30-7 SDS

1867-30-7Downstream Products

1867-30-7Relevant academic research and scientific papers

Design, synthesis, DFT, docking studies and ADME prediction of some new coumarinyl linked pyrazolylthiazoles: Potential standalone or adjuvant antimicrobial agents

Kumar, Sunil,Saini, Vikram,Maurya, Indresh K.,Sindhu, Jayant,Kumari, Mukesh,Kataria, Ramesh,Kumar, Vinod

, (2018/04/30)

The control of antimicrobial resistance (AMR) seems to have come to a dead end. The major consequences of the use and abuse of antibacterial drugs are the development of resistant strains due to genetic mutability of both pathogenic and nonpathogenic microorganisms. We, herein, report the synthesis, characterization and biological activities of coumarin-thiazole-pyrazole (CTP) molecular hybrids with an effort to explore and overcome the increasing antimicrobial resistance. The compounds were characterized by analyzing their IR, Mass, 1H and13C NMR spectral data and elemental analysis. The in vitro antimicrobial activity of the synthesized compounds was investigated against various pathogenic strains; the results obtained were further explained with the help of DFT and molecular orbital calculations. Compound 1b and 1f displayed good antimicrobial activity and synergistic effects when used with kanamycin and amphotericin B. Furthermore, in vitro cytotoxicity of compounds 1b and 1f were studied against HeLa cells (cervical cancer cell) and Hek-293 cells. The results of molecular docking study were used to better rationalize the action and prediction of the binding modes of these compounds.

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