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2-[bis-(4-chlorophenyl)methyl]-1-phenylbutane-1,3-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

445395-20-0

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445395-20-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 445395-20-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,5,3,9 and 5 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 445395-20:
(8*4)+(7*4)+(6*5)+(5*3)+(4*9)+(3*5)+(2*2)+(1*0)=160
160 % 10 = 0
So 445395-20-0 is a valid CAS Registry Number.

445395-20-0Downstream Products

445395-20-0Relevant academic research and scientific papers

Synthesis and structure of an air-stable bis(isopropylcyclopentadienyl) zirconium perfluorooctanesulfonate and its catalyzed benzylation of 1,3-dicarbonyl derivatives with alcohols

Zhang, Xiaohong,Qiu, Renhua,Zhou, Congcong,Yu, Jingxing,Li, Ningbo,Yin, Shuangfeng,Xu, Xinhua

, p. 1011 - 1017 (2015)

An air-stable uninuclear complex of bis(isopropylcyclopentadienyl) zirconium perfluorooctane sulfonate (1a·H2O·3THF) was successfully synthesized by the reaction of (i-PrCp)2ZrCl2 with C17SO3Ag. The c

Fe2(SO4)3·xH2O on silica: An efficient and low-cost catalyst for the direct nucleophilic substitution of alcohols in solvent-free conditions

Li, Lingjun,Zhu, Anlian,Zhang, Yuqin,Fan, Xincui,Zhang, Guisheng

, p. 4286 - 4291 (2014/01/17)

Fe2(SO4)3·xH2O on silica has been found to be a novel efficient catalyst for the direct nucleophilic substitution of alcohols in solvent-free conditions. In this reaction system, the alcohols can react with various nucleophilic reagents for the convenient construction of C-C bonds and C-N bonds with the benefits of high conversion, no requirement to use excessive amounts of the nucleophile, only a catalytic amount of iron catalyst required, solvent-free and benign reaction conditions, and the feasible reusability of the catalyst.

Direct nucleophilic substitution reaction of alcohols mediated by a zinc-based ionic liquid

Zhu, Anlian,Li, Lingjun,Wang, Jianji,Zhuo, Kelei

experimental part, p. 1244 - 1250 (2011/06/26)

A zinc-based ionic liquid ([CHCl][ZnCl2]2) was found to be an excellent reaction medium for the direct nucleophilic substitution reactions of alcohols. The high conversion, high selectivity, easy separation procedure, catalyst reusability and no necessity of excessive nucleophiles make the chemical process cleaner. This reaction was believed to work through the carbocation mechanism and the existence of carbocation was detected by UV-vis spectroscopy. It was suggested that the hydroxyl group on the choline cation was the major inducement for the formation of special microstructures which could provide adequate stability for the carbocation in the reaction systems and increase the reactivity and selectivity.

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