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2-((E)-(((E)-4-phenylthiazol-2(3H)-ylidene)hydrazono)methyl)phenol is a complex organic compound characterized by its unique molecular structure. It features a phenol group attached to aazon hydro-methyl moiety, which in turn is connected to a thiazol-2(3H)-ylidene system. The compound exhibits two (E)-configurations, indicating that the double bonds within the molecule are arranged in a specific geometric pattern. This chemical is primarily of interest in the field of organic chemistry, where it may be studied for its potential applications in the synthesis of pharmaceuticals, dyes, or other specialty chemicals. Its specific properties, such as solubility, reactivity, and stability, would be of particular interest to researchers and chemists working in these areas.

21938-33-0

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21938-33-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21938-33-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,9,3 and 8 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 21938-33:
(7*2)+(6*1)+(5*9)+(4*3)+(3*8)+(2*3)+(1*3)=110
110 % 10 = 0
So 21938-33-0 is a valid CAS Registry Number.

21938-33-0Relevant academic research and scientific papers

Efficient one-pot three-component synthesis of N-(4-arylthiazol-2-yl) hydrazones in water under ultrasound irradiation

Zhang, Dong-Nuan,Li, Ji-Tai,Song, Ya-Li,Liu, Hui-Min,Li, Hong-Ya

experimental part, p. 475 - 478 (2012/04/23)

A highly efficient and facile one-pot three-component synthesis of N-(4-arylthiazol-2-yl) hydrazones was carried out in excellent yield without any catalyst in water under ultrasound irradiation.

Synthesis, antibacterial activity and quantum-chemical studies of novel 2-arylidenehydrazinyl-4-arylthiazole analogues

Alam, Mohammad Sayed,Liu, Lijun,Lee, Yong-Eok,Lee, Dong-Ung

, p. 568 - 573 (2011/06/24)

A new series of 2-arylidenehydrazinyl-4-arylthiazole derivatives (2a-k) was designed and synthesized through a rapid, simple, and efficient methodology in excellent isolated yield. These compounds were screened for in vitro antimicrobial activities against eight bacteria, e.g. Bacillus cereus, Staphylococcus aureus, Bacillus subtilis, Bacillus megaterium, Pseudomonas aeruginosa, Shigella dysenteriae, Salmonella typhi, Escherichia coli, and three fungi e.g. Aspergillus oryzae, Candida albicans, and Saccharomyces cerevis. The results indicate that some of the compounds exhibit strong antibacterial activity, depending on the bacterial strain, but show virtually no antifungal activity. The structure-antibacterial activity relationships were studied using some physicochemical and quantum-chemical parameters with the ab initio Hartree-Fock model at the RHF/6-31G level of theory. A good qualitative correlation between predicted lipophilic parameters and antibacterial activity has been found.

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