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N-[(1E)-1-methylpent-1-enyl]-N-phenyl-5H-dibenzo[b,f]-azepine-5-carboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1369960-34-8

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1369960-34-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1369960-34-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,9,9,6 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1369960-34:
(9*1)+(8*3)+(7*6)+(6*9)+(5*9)+(4*6)+(3*0)+(2*3)+(1*4)=208
208 % 10 = 8
So 1369960-34-8 is a valid CAS Registry Number.

1369960-34-8Downstream Products

1369960-34-8Relevant academic research and scientific papers

Synthesis of a carbamazepine derivative as antibacterial agent

Figueroa-Valverde, Lauro,Díaz-Cedillo, Francisco,Garcia-Cervera, Elodia,Pool-Gómez, Jose E.M.,Carde?a-Arredondo, Carlos

experimental part, p. 699 - 704 (2012/09/10)

In this work, the carbamazepine derivative (N-[(1E)-1-methylpent-1-enyl]-N- phenyl-5H-dibenzo[b,f]azepine-5-carboxamide) was synthesized using the three-component system (carbamazepine, benzaldehyde and 2-hexyne) in presence of cupric chloride as catalyst. Additionally, the antibacterial activity of carbamazepine derivative was evaluated in vitro on S. aureus and E. coli using the NCCLS method with some modifications. To delineate the structural chemical requirements of the compound N-[(1E)-1-methylpent-1-enyl]-N- phenyl-5H-dibenzo[b,f]azepine-5-carboxamide as antibacterial agents on S. aureus and E. coli, other chemical parameters such as the descriptors log P, π, Rm, Vm, Pc and St were calculated. The results showed that bacterial growth of the microorganisms studied was inhibited by the carbamazepine derivative in a dose-dependent manner. Other results showed an increase in log P, π, Rm, Vm, P c and St values in comparison with carbamazepine. These data suggest that functional groups involved in the structure of the studied compound are specific for its antibacterial activity.

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