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5-benzyl-2,4-diphenylthiazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

59824-82-7

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59824-82-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59824-82-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,8,2 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 59824-82:
(7*5)+(6*9)+(5*8)+(4*2)+(3*4)+(2*8)+(1*2)=167
167 % 10 = 7
So 59824-82-7 is a valid CAS Registry Number.

59824-82-7Relevant academic research and scientific papers

Polysubstituted 2, 4 - diarylthiazole and derivatives and synthesis method thereof

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Paragraph 0047-0053; 0055-0056; 0111, (2021/10/27)

The invention relates to a synthesis method of polysubstituted 2,4-diaryl thiazole and derivatives thereof. With the technical scheme that aromatic ketone compounds, aromatic aldehyde compounds, ammonium salts and sulfur powder are developed for the first

Four-component thiazole formation from simple chemicals under metal-free conditions

Jiang, Jingjing,Huang, Huawen,Deng, Guo-Jun

supporting information, p. 986 - 990 (2019/03/12)

Multi-component reactions for the synthesis of polysubstituted thiazoles from simple chemicals are described. Under metal-free reaction conditions, cheap and easily available ketones, aldehydes, ammonium salt, and elemental sulfur are self-assembled to provide entries to three thiazoles in moderate to good yield with a range of functionalities tolerated.

Facile one-pot synthesis of three different substituted thiazoles from propargylic alcohols

Gao, Xun,Pan, Ying-Ming,Lin, Min,Chen, Li,Zhan, Zhuang-Ping

supporting information; experimental part, p. 3259 - 3266 (2010/08/21)

Three different substituted thiazoles have been successfully synthesized from readily available propargylic alcohols. Various secondary propargylic alcohols or tertiary propargylic alcohols participated well in the reaction, providing the desired products in good yields. This method provides a flexible and rapid route to substituted thiazoles. The Royal Society of Chemistry 2010.

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