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2,2-bis(2-chlorophenyl)acetaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51559-01-4

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51559-01-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51559-01-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,5,5 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 51559-01:
(7*5)+(6*1)+(5*5)+(4*5)+(3*9)+(2*0)+(1*1)=114
114 % 10 = 4
So 51559-01-4 is a valid CAS Registry Number.

51559-01-4Relevant academic research and scientific papers

Highly regioselective rearrangement of 2,3-diaryl-oxiranes into 2,2-diarylacetaldehydes catalyzed by ytterbium porphyrin complex, Yb(TPP)OTf

Takanami, Toshikatsu,Nakajima, Shin-ichiro,Nakadai, Shoichi,Hino, Fumio,Suda, Kohji

experimental part, p. 365 - 374 (2009/09/06)

[5,10,15,20-Tetraphenylporphynato]ytterbium(III) triflate, Yb(TPP)-OTf, is an efficient Lewis acid catalyst for the highly regioselective rearrangement of 2,3-diaryloxiranes into 2,2-diarylacetaldehydes. The catalytic process can be easily performed not only in dichloroethane but also in a more environmentally friendly solvent, benzotrifluoride.

Tandem pinacol coupling-rearrangement of aromatic aldehydes with hydrogen catalyzed by a combination of a platinum complex and a polyoxometalate

Branytska, Olena,Shimon, Linda J. W.,Neumann, Ronny

, p. 3957 - 3959 (2008/10/09)

Together with a strongly oxidizing polyoxometalate, H5PV 2Mo10O40, PtII(N-(2,6- diisopropylphenyl)pyrazin-2-ylmethanimine)Cl2 forms a combined catalyst that was active in the tandem pinacol coupling-rearrangement of aryl aldehydes to give mostly the corresponding diarylacetaldehyde in high yields using molecular hydrogen as the reducing agent. The Royal Society of Chemistry.

Synthesis and structure-activity relationship studies of novel 2-diarylethyl substituted (2-carboxycycloprop-1-yl)glycines as high-affinity group II metabotropic glutamate receptor ligands.

Sorensen, Ulrik S,Bleisch, Thomas J,Kingston, Anne E,Wright, Rebecca A,Johnson, Bryan G,Schoepp, Darryle D,Ornstein, Paul L

, p. 197 - 205 (2007/10/03)

The major excitatory neurotransmitter in the central nervous system, (S)-glutamic acid , activates both ionotropic and metabotropic excitatory amino acid receptors. Its importance in connection to neurological and psychiatric disorders has directed great

Synthesis of novel GABA uptake inhibitors. 3. Diaryloxime and diarylvinyl ether derivatives of nipecotic acid and guvacine as anticonvulsant agents

Knutsen, Lars J. S.,Andersen, Knud Erik,Lau, Jesper,Lundt, Behrend F.,Henry, Rodger F.,Morton, Howard E.,N?rum, Lars,Petersen, Hans,Stephensen, Henrik,Suzdak, Peter D.,Swedberg, Michael D. B.,Thomsen, Christian,S?rensen, Per O.

, p. 3447 - 3462 (2007/10/03)

(3R)-1-[4,4-bis(3-methyl-2-thienyl)-3-butenyl]-3-piperidinecarboxylic acid 1 (tiagabine, Gabitril) is a potent and selective γ-aminobutyric acid (GABA) uptake inhibitor with proven anticonvulsant efficacy in humans. This drug, which has a unique mechanism

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