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Benzamide, 3,4,5-trimethoxy-N-(4-methoxyphenyl)-, also known as 3,4,5-trimethoxy-N-(4-methoxyphenyl)benzamide, is a complex organic compound with the molecular formula C17H19NO5. It is a derivative of benzamide, featuring a benzene ring with three methoxy groups (-OCH3) attached at the 3, 4, and 5 positions, and a 4-methoxyphenyl group (-C6H4OCH3) connected to the nitrogen atom through an amide linkage. Benzamide, 3,4,5-trimethoxy-N-(4-methoxyphenyl)- is characterized by its unique structure and potential applications in various fields, such as pharmaceuticals and materials science, due to its specific chemical properties and reactivity.

742-15-4

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742-15-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 742-15-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,4 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 742-15:
(5*7)+(4*4)+(3*2)+(2*1)+(1*5)=64
64 % 10 = 4
So 742-15-4 is a valid CAS Registry Number.

742-15-4Relevant academic research and scientific papers

Stable and Reusable Binaphthyl-Supported Palladium Catalyst for Aminocarbonylation of Aryl Iodides

Sharma, Nidhi,Sekar, Govindasamy

supporting information, p. 314 - 320 (2016/02/14)

A binaphthyl-supported Pd nanoparticles (Pd-BNP)-catalyzed aminocarbonylation of aryl iodides in the presence of carbon monoxide and amines for the synthesis of amides has been developed. This methodology provides an efficient route for the synthesis of a COX-2 enzyme inhibitor having anti-inflammatory activity.

Discovery of 4-amino and 4-hydroxy-1-aroylindoles as potent tubulin polymerization inhibitors

Liou, Jing-Ping,Wu, Zi-Yi,Kuo, Ching-Chuan,Chang, Chi-Yen,Lu, Pei-Yi,Chen, Chi-Ming,Hsieh, Hsing-Pang,Chang, Jang-Yang

supporting information; experimental part, p. 4351 - 4355 (2009/05/26)

1-Aroylindoline, 1-aroyl-1,2,3,4-tetrahydroquinoline, and 1-aroylindole derivatives were synthesized and evaluated for anticancer activity. The 4-amino and 4-hydroxy-1-aroylindoles 26 and 27 with IC50 of 0.9 and 0.6 μM, respectively, exhibited

Highly potent triazole-based tubulin polymerization inhibitors

Zhang, Qiang,Peng, Youyi,Wang, Xin I.,Keenan, Susan M.,Arora, Sonia,Welsh, William J.

, p. 749 - 754 (2007/10/03)

We describe the synthesis and biological evaluation of a series of tubulin polymerization inhibitors that contain the 1,2,4-triazole ring to retain the bioactive configuration afforded by the cis double bond in combretastatin A-4 (CA-4). Several of the su

ANTI-MITOTIC ANTI-PROLIFERATIVE COMPOUNDS

-

Page/Page column 13-14; 25, (2008/06/13)

Substituted triazole compounds and pharmaceutical compositions thereof are presented. Also presented are methods for treating a pathology linked to a hyperproliferative disorder by administering the substituted triazole compounds to a patient in need ther

Stilbene derivatives as anticancer agents

-

, (2008/06/13)

The present invention relates to stilbene derivatives which possess utility as anti-cancer agents. The compounds can be used to treat cancers which are susceptible to treatment therewith, and can be utilized in a method of treating such cancers. Pharmaceu

Synthesis and Evaluation of Stilbene and Dihydrostilbene Derivatives as Potential Anticancer Agents That Inhibit Tubulin Polymerization

Cushman, Mark,Nagarathnam, Dhanapalan,Gopal, D.,Chakraborti, Asit K.,Lin, Chii M.,Hamel, Ernest

, p. 2579 - 2588 (2007/10/02)

An array of cis-, trans-, and dihydrostilbenes and some N-arylbenzylamines were synthesized and evaluated for their cytotoxicity in the five cancer cell cultures A-549 lung carcinoma, MCF-7 breast carcinoma, HT-29 colon adenocarcinoma, SKMEL-5 melanoma, a

Synthesis and CNS-depressant profile of 3,4,5-trimethoxybenzoyl analogues

Kar

, p. 313 - 315 (2007/10/02)

A series of 3,4,5-trimethoxybenzoyl analogues with varying electronic and stereochemical characteristics has been synthesized. Many of these compounds (4, 5, 9, 12, 15) showed appreciable potentiation of pentobarbitone-induced hypnosis. Several analogues (1, 5, 6, 11, 12, 15) exhibited marked reduction of spontaneous motor activity (SMA).

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