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N-(4-((4-carboxyphenyl)(4-(dimethylamino)phenyl)methylene)cyclohexa-2,5-dien-1-yliden)-N-methylmethanaminium chloride is a complex organic compound with the molecular formula C26H26ClN2O2. It is a derivative of a phenylmethylene-cyclohexa-2,5-dien-1-yliden-N-methylmethanaminium structure, featuring a cyclohexa-2,5-dien-1-yliden group connected to a phenyl ring through a methylene bridge. The phenyl ring is further substituted with a carboxyphenyl group and a dimethylaminophenyl group. N-(4-((4-carboxyphenyl)(4-(dimethylamino)phenyl)methylene)cyclohexa-2,5-dien-1-yliden)-N-methylmethanaminium chloride is characterized by its unique structure, which includes a cyclohexadienylidenemethanaminium core, a carboxyphenyl group, and a dimethylaminophenyl group, all contributing to its chemical properties and potential applications in various fields, such as pharmaceuticals or materials science.

6362-26-1

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6362-26-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6362-26-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,6 and 2 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6362-26:
(6*6)+(5*3)+(4*6)+(3*2)+(2*2)+(1*6)=91
91 % 10 = 1
So 6362-26-1 is a valid CAS Registry Number.

6362-26-1Downstream Products

6362-26-1Relevant academic research and scientific papers

Synthesis and cytotoxic evaluation of malachite green derived oleanolic and ursolic acid piperazineamides

Csuk, René,Friedrich, Sander,Hoenke, Sophie,Serbian, Immo,Wolfram, Ratna Kancana

, p. 926 - 933 (2020/04/23)

The coupling of acetylated piperazinylamide spacered triterpenoic oleanolic acid and ursolic acid with meta or para substituted carboxylated malachite green analogs gave conjugates 10, 11, 15, and 16 that were cytotoxic for several human tumor cell lines. Especially, an oleanolic acid-derived compound 10 was cytotoxic for MCF-7 human breast carcinoma cells (EC50 = 0.7 μM). These derivatives represent first examples of triterpenoic acid derivatives holding a cationic scaffold derived from malachite green. [Figure not available: see fulltext.]

Production of antibodies for selective detection of malachite green and the related triphenylmethane dyes in fish and fishpond water

Yang, Mei-Chun,Fang, Jim-Min,Kuo, Tzong-Fu,Wang, Da-Ming,Huang, Yi-Lin,Liu, Liang-Yirn,Chen, Pen-Heng,Chang, Tong-Hsuan

experimental part, p. 8851 - 8856 (2009/09/29)

This study provides a practical method for production of the antibodies against malachite green (MG) and its primary metabolite leucomalachite green (LMG). Two ELISA kits are constructed with the MG and LMG antibodies for detection of the residual MG and LMG in fish muscle and fishpond water. The detection limit is established at the level of 0.05 μg/L for both MG and LMG. Our ELISA kits show the advantages of good specificity, high sensitivity, and convenience in rapid screening of MG and LMG residues. The sample of fishpond water, without extraction or prior preparation, is directly assayed by the ELISA kit. More then 80 fish samples can be simultaneously tested in a kit. The toxic crystal violet and its metabolite leucocrystal violet of illegal use in aquaculture are detected by our prepared MG and LMG antibodies, whereas the antibodies do not cross-react with common antibiotics, sulfonamides, and benzene derivatives.

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