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4-(2-(4-chlorophenyl)hydrazineylidene)-3-methyl-5-oxo-4,5-dihydro-1H-pyrazole-1-carbothiohydrazide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

876344-77-3

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876344-77-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 876344-77-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,6,3,4 and 4 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 876344-77:
(8*8)+(7*7)+(6*6)+(5*3)+(4*4)+(3*4)+(2*7)+(1*7)=213
213 % 10 = 3
So 876344-77-3 is a valid CAS Registry Number.

876344-77-3Downstream Products

876344-77-3Relevant academic research and scientific papers

Design, synthesis, and antimicrobial evaluation of novel pyrazoles and pyrazolyl 1,3,4-thiadiazine derivatives

Radini, Ibrahim Ali M.

, (2018)

A novel series of pyrazolyl 1,3,4-thiadiazines 5a–c, 8a–c, 12, 15a–c, 17a–c, and 20 was prepared from the reaction of pyrazole-1-carbothiohydrazide 1a,b with 2-oxo-N0-arylpropanehydrazonoyl chloride, 2-chloro-2-(2-arylhydrazono)acetate, and 3-bromoacetylcoumarin. Moreover, the regioselective reaction of 5-pyrazolone-1- carbothiohydrazide 1a with 4-substituted diazonium salts and 4-(dimethylamino)benzaldehyde gave the corresponding hydrazones 21a–c and 22. The newly prepared compounds were characterized by spectroscopy and elemental analysis. Many new synthesized compounds showed considerable antimicrobial activity against tested microorganisms. Hydrazones 21a–c and 22 showed remarkable antibacterial and antifungal activities. 4-(2-(p-tolyl) hydrazineylidene)-pyrazole-1-carbothiohydrazide 21a displayed the highest antibacterial and antifungal activities with minimum inhibitory concentration (MIC) values lower than standard drugs chloramphenicol and clotrimazole, in the range of 62.5–125 and 2.9–7.8 μg/mL, respectively.

Synthesis of some substituted pyrazolones

Dabholkar, Vijay V.,Hawaldar, Freddy,Khapare, Sachin

experimental part, p. 249 - 252 (2011/12/15)

Ethyl-2-[diazo (substituted benzene)] acetoacetates II were treated with thiosemicarbazide to furnish 4-(substituted phenyl) azo-5-methyl-2-thioamido-3- pyrazolones III. Compounds II on treatment with one molar quantity of thiocarbohydrazide (TCH) yielded 4-(substituted phenyl) azo-5-methyl-2- thiocarboxyhydrazino-3-pyrazolones IV whereas bis-2-[4-(substituted phenyl) azo-5-methyl-3-pyrazolone] thioketones V were obtained by treating II with two molar quantity of TCH. All the final desired compounds have been synthesized by microwave irradiation technique as well as classical thermal method. The structures of the newly synthesized compounds have been established by analytical and spectral methods.

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