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4-((E)-3-Oxo-but-1-enyl)-benzoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

181214-91-5

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181214-91-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 181214-91-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,1,2,1 and 4 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 181214-91:
(8*1)+(7*8)+(6*1)+(5*2)+(4*1)+(3*4)+(2*9)+(1*1)=115
115 % 10 = 5
So 181214-91-5 is a valid CAS Registry Number.

181214-91-5Downstream Products

181214-91-5Relevant academic research and scientific papers

Palladium nanoparticles supported on copper oxide as an efficient and recyclable catalyst for carbon(sp2)-carbon(sp2) cross-coupling reaction

Nasrollahzadeh, Mahmoud,Sajadi, S. Mohammad,Rostami-Vartooni, Akbar,Azarian, Abbas

, p. 150 - 154 (2015/04/14)

A convenient, mild and cost-effective synthesis of Pd/CuO nanoparticles by arc discharge of Cu in deionized (DI) water and electroless deposition of palladium was reported. The obtained nanoparticles were thoroughly characterized by using techniques like TEM, XRD, FE-SEM and EDS. The synthesized nanoparticles demonstrated excellent catalytic activity in Heck coupling reaction under aerobic conditions. The effects of catalyst composition, solvent and bases, aryl halides or olefins species on corresponding products were systematically investigated. High product yields, elimination of ligand and homogeneous catalysts, broad substrate scope and easy work up are important features of this method. In addition, the catalyst could be reused for five more consecutive recycles.

Benzoyl 2-methyl indoles as selective PPARγ modulators

Acton III, John J.,Black, Regina M.,Jones, A. Brian,Moller, David E.,Colwell, Lawrence,Doebber, Thomas W.,MacNaul, Karen L.,Berger, Joel,Wood, Harold B.

, p. 357 - 362 (2007/10/03)

A series of selective PPARγ modulators (SPPARγMs) and their development from hPPARγ active screening leads 1 and 2 is described. SPPARγM 24 displayed robust anti-diabetic activity with an improved therapeutic window in comparison to a PPARγ full agonist in a rodent efficacy model. Routine screening for human PPAR ligands yielded compounds 1 and 2, both of which were sub-micromolar hPPARγ agonists. Synthetic modifications of these leads led to a series of potent substituted 3-benzyl-2-methyl indoles, a subset of which were noted to be selective PPARγ modulators (SPPARγMs). SPPARγM 24 displayed robust anti-diabetic activity with an improved therapeutic window in comparison to a PPARγ full agonist in a rodent efficacy model.

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