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5-methylphenanthridinium chloride is a chemical compound with the molecular formula C15H13ClN2. It is a derivative of phenanthridine, a tricyclic aromatic compound, with a methyl group attached at the 5th position. 5-methylphenanthridinium chloride is known for its potential applications in various fields, including pharmaceuticals and materials science. It is often used as an intermediate in the synthesis of other organic compounds and may exhibit biological activity, making it a subject of interest in chemical research. The chloride salt form of 5-methylphenanthridinium is soluble in water and can be used in various chemical reactions due to its cationic nature.

65201-98-1

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65201-98-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65201-98-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,2,0 and 1 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 65201-98:
(7*6)+(6*5)+(5*2)+(4*0)+(3*1)+(2*9)+(1*8)=111
111 % 10 = 1
So 65201-98-1 is a valid CAS Registry Number.

65201-98-1Downstream Products

65201-98-1Relevant academic research and scientific papers

Synthesis and antibacterial activity of 5-methylphenanthridium derivatives as FtsZ inhibitors

Liu, Fang,Venter, Henrietta,Bi, Fangchao,Semple, Susan J.,Liu, Jingru,Jin, Chaobin,Ma, Shutao

, p. 3399 - 3402 (2017/07/07)

5-Methylphenanthridium derivatives were designed, synthesized and evaluated for their in vitro antibacterial activity and cell division inhibitory activity against various Gram-positive and -negative bacteria. Among them, compounds 5A2, 5B1, 5B2, 5B3, 5C1 and 5C2 displayed the best on-target antibacterial activity with an MIC value of 4?μg/mL against B. subtilis ATCC9372 and S. pyogenes PS, showing over 2-fold better activity than sanguinarine. The SARs showed that the 5-methylphenanthridium derivatives with the alkyl side chains at the 2-postion, especially the straight alkyl side chains exerted better on-target antibacterial activity.

Synthesis of 5-methyl phenanthridium derivatives: A new class of human DOPA decarboxylase inhibitors

Cheng, Pi,Zhou, Jie,Qing, Zhixing,Kang, Weisong,Liu, Sheng,Liu, Wei,Xie, Hongqi,Zeng, Jianguo

, p. 2712 - 2716 (2014/06/09)

DOPA decarboxylase (DDC) is responsible for the decarboxylation of l-DOPA and related aromatic amino acids and correlates closely with a number of clinical disorders. Sanguinarine, a natural quaternary benzophenanthridine alkaloid (QBA), was reported to b

Synthesis of 5-methyl phenanthridium derivatives: A new class of human DOPA decarboxylase inhibitors

Cheng, Pi,Zhou, Jie,Qing, Zhixing,Kang, Weisong,Liu, Sheng,Liu, Wei,Xie, Hongqi,Zeng, Jianguo

, p. 2712 - 2716 (2015/02/19)

DOPA decarboxylase (DDC) is responsible for the decarboxylation of l-DOPA and related aromatic amino acids and correlates closely with a number of clinical disorders. Sanguinarine, a natural quaternary benzophenanthridine alkaloid (QBA), was reported to b

KINETICS OF HYDRIDE TRANSFER BETWEEN NITROGEN HETEROAROMATIC CATIONS

Bunting, John W.,Luscher, Mark A.

, p. 2524 - 2531 (2007/10/02)

The kinetics of the reduction of the 3-cyano-1-methylquinolinium, 4-cyano-2-methylisoquinolinium, and 2-methyl-5-nitroisoquinolinium cations by 9,10-dihydro-10-methylacridine, and also the reduction of these same three cations as well as the 10-methylacridinium cation by 5,6-dihydro-5-methylphenanthridine, have been investigated in 20percent acetonitrile - 80percent water, ionic strength 1.0, 25 deg C.The reactions of the 2-methyl-5-nitroisoquinolinium cation with both reductants, and also of the 4-cyano-2-methylisoquinolinium cation with 9,10-dihydro-10-methylacridine, display kinetic saturation effects in the pseudo-first-order rate constants as a function of heterocyclic cation concentration.These effects are consistent with the formation of 1:1 association complexes between hydride donor and acceptor prior to the rate-determining step of the reduction.The second-order rate constants for these reactions, and also those for analogous heterocyclic cation reductions by 1,4-dihydronicotinamides, show systematic variations as a function of the hydride donor and acceptor species.

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