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Benzoic acid, 2-[(methylamino)carbonyl]hydrazide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

50369-40-9

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50369-40-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50369-40-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,3,6 and 9 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 50369-40:
(7*5)+(6*0)+(5*3)+(4*6)+(3*9)+(2*4)+(1*0)=109
109 % 10 = 9
So 50369-40-9 is a valid CAS Registry Number.

50369-40-9Relevant academic research and scientific papers

Synthesis, characterization and antioxidant activities of semicarbazide and thiosemicarbazide derivatives

Alam, Faima,Ali, Basharat,Ali, Mahboob,Khan, Khalid Mohammed,Khan, Momin,Manaf, Abdul,Zaman, Khair

, p. 475 - 483 (2021/08/21)

In this research work Semicarbazide, thiosemicarbazide derivatives 3 to 25 were synthesized by conventional methods with high percentage yield and reaction rate. 1H-NMR and EIMS spectroscopic techniques were used to elucidate the structure of t

PYRIDOPYRIMIDINES AND METHODS OF THEIR USE

-

Page/Page column 76, (2021/12/28)

Disclosed are compounds useful in the treatment of neurological disorders. The compounds described herein, alone or in combination with other pharmaceutically active agents, can be used for treating or preventing neurological diseases.

2,4-Dihydro-3H-1,2,4-triazol-3-ones as anticonvulsant agents

Kane,Baron,Dudley,Sorensen,Staeger,Miller

, p. 2772 - 2777 (2007/10/02)

A series of 5-aryl-2,4-dihydro-3H-1,2,4-triazol-3-ones was evaluated for anticonvulsant activity. In general the members of this series were prepared by the alkaline crystalization of 1-aroyl-4-alkylsemicarbazides. The resulting 2-unsubstituted 3H-1,2,4-t

The Bis(tricyclohexylstannyl) Sulfide Thionation of 3H-1,2,4-Triazol-3-ones

Kane, John M.

, p. 912 - 914 (2007/10/02)

5-Aryl-2,4-dialkyl-2,4-dihydro-3H-1,2,4-triazol-3-ones may be converted in 55-74percent yield to the corresponding 3H-1,2,4-triazole-3-thiones by using the combination bis(tricyclohexylstannyl) sulfide/boron trichloride.

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