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1-(3-chlorophenyl)-2-p-tolylethane-1,2-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

955016-79-2

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955016-79-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 955016-79-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,5,0,1 and 6 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 955016-79:
(8*9)+(7*5)+(6*5)+(5*0)+(4*1)+(3*6)+(2*7)+(1*9)=182
182 % 10 = 2
So 955016-79-2 is a valid CAS Registry Number.

955016-79-2Downstream Products

955016-79-2Relevant academic research and scientific papers

A combination of copper(0) powder and selectfluor enables generation of cationic copper species for mild 1,2-dicarbonylation of alkynes

Zhang, Wenxia,Zhang, Jian,Liu, Yunkui,Xu, Zhenyuan

supporting information, p. 2709 - 2714 (2014/01/06)

A combination of copper powder and Selectfluor permits the generation of cationic copper species that efficiently catalyze 1,2-dicarbonylation of alkynes under mild conditions with water and dioxygen as inexpensive and environmentally benign sources of oxygen. Georg Thieme Verlag Stuttgart New York.

Synthesis, antileukemic and antiplatelet activities of 2,3-diaryl-6,7-dihydro-5H-1,4-diazepines

Ramajayam,Giridhar, Rajani,Yadav,Balaraman,Djaballah, Hakim,Shum, David,Radu, Constantin

, p. 2004 - 2010 (2008/12/22)

The synthesis, antileukemic and antiplatelet activity evaluation of 2,3-diaryl-6,7-dihydro-5H-1,4-diazepines are described. In general, it was found that compound 17o showed moderate antileukemic activity against MOLT3 human leukemic cancer cell lines. An arachidonic acid induced platelet aggregation effect on washed rat platelets was studied. Compound 17i was found to be the most potent. The antiplatelet properties may be mediated by interference with the arachidonic acid pathway.

Synthesis of novel substituted diaryl-1,4-diazepines

Ramajayam,Giridhar, Rajani,Yadav

, p. 901 - 906 (2008/02/12)

In this paper a convenient route to new 2,3-diaryl-substituted 1,4-diazepines is described through cyclization of ethanedione derivatives and 1,3-propanediamine. The ethanedione derivatives required were synthesized by microwave-assisted oxidation from ethanones.

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