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methyl 3-(3-nitrophenyl)-3-oxo-2-(triphenylphosphoranylidene)propanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

96869-84-0

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96869-84-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96869-84-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,8,6 and 9 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 96869-84:
(7*9)+(6*6)+(5*8)+(4*6)+(3*9)+(2*8)+(1*4)=210
210 % 10 = 0
So 96869-84-0 is a valid CAS Registry Number.

96869-84-0Relevant academic research and scientific papers

Palladium-Catalyzed Ylidyl-Carbonylation of Aryl Halides to Produce α-Acylphosphoranes

Guo, Xiaojun,Ma, Wei,Xue, Dong,Wang, Chao,Xiao, Jianliang

supporting information, p. 4824 - 4827 (2016/10/14)

An efficient synthesis of α-acylphosphoranes by palladium-catalyzed carbonylation of aryl iodides with carbon monoxide and stabilized phosphonium ylides has been developed. Featuring 44 examples, the protocol displayed a wide substrate scope under mild reaction conditions, showcasing its potential in synthetic organic chemistry.

Selective inhibitors of the protein tyrosine phosphatase SHP2 block cellular motility and growth of cancer cells in vitro and in vivo

Grosskopf, Stefanie,Eckert, Chris,Arkona, Christoph,Radetzki, Silke,B?hm, Kerstin,Heinemann, Udo,Wolber, Gerhard,Von Kries, Jens-Peter,Birchmeier, Walter,Rademann, J?rg

, p. 815 - 826 (2015/05/05)

Selective inhibitors of the protein tyrosine phosphatase SHP2 (src homology region 2 domain phosphatase; PTPN11), an enzyme that is deregulated in numerous human tumors, were generated through a combination of chemical synthesis and structure-based ration

Synthesis of 2-amino-6-phenyl-4H-pyran-4-ones

Morris,Wishka

, p. 43 - 46 (2007/10/02)

The treatment of a series of phenylacetylenic β-keto amides with methanesulfonic acid produces a high yielding intramolecular cyclization to the corresponding 2-amino-6-phenyl-4H-pyran-4-ones.

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