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62373-05-1

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62373-05-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62373-05-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,3,7 and 3 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 62373-05:
(7*6)+(6*2)+(5*3)+(4*7)+(3*3)+(2*0)+(1*5)=111
111 % 10 = 1
So 62373-05-1 is a valid CAS Registry Number.

62373-05-1Downstream Products

62373-05-1Relevant articles and documents

Synthesis and in vitro antimicrobial activity of new 4-phenyl-5-methyl-4H-1,2,4-triazole-3-thione derivatives

Popiolek, Lukasz,Kosikowska, Urszula,Dobosz, Maria,Malm, Anna

, p. 479 - 488 (2015/02/19)

This study presents the synthesis, spectral analysis and antimicrobial evaluation of a new series of substituted 1,2,4-triazole (5a-i) and 1,3,4-thiadiazole derivatives (9a, c, g, h). New compounds were obtained by cyclization reaction of acyl thiosemicarbazide derivatives in the presence of alkaline and acidic media. All synthesized compounds were screened for their in vitro antimicrobial activities. Nine of the compounds had potential activity against Gram-positive bacteria (MIC = 3.91-500 μg/mL). Some compounds showed good activity especially against: Micrococcus luteus ATCC 10240 (MIC = 3.91-31.25 μg/mL), Bacillus subtilis ATCC 6633 (MIC = 15.63-62.5 μg/mL), and Staphylococcus aureus ATCC 25923 (MIC = 15.63-125 μg/mL).

Synthesis and in vitro antimicrobial activity of new 4-phenyl-5-methyl-4H- 1,2,4-triazole-3-thione derivatives

Popiolek, Ukasz,Kosikowska, Urszula,Dobosz, Maria,Malm, Anna

, p. 479 - 488 (2013/05/08)

This study presents the synthesis, spectral analysis and antimicrobial evaluation of a new series of substituted 1,2,4-triazole (5a-i) and 1,3,4-thiadiazole derivatives (9a, c, g, h). New compounds were obtained by cyclization reaction of acyl thiosemicarbazide derivatives in the presence of alkaline and acidic media. All synthesized compounds were screened for their in vitro antimicrobial activities. Nine of the compounds had potential activity against Gram-positive bacteria (MIC=3.91-500 g/mL). Some compounds showed good activity especially against: Micrococcus luteus ATCC 10240 (MIC=3.91-31.25 g/mL), Bacillus subtilis ATCC 6633 (MIC=15.63- 62.5 /mL), and Staphylococcus aureus ATCC 25923 (MIC=15.63-125 g/mL).

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