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(2R)-2-methoxy-3-{4-[2-(5-methyl-2-phenyl-oxazol-4-yl)-ethoxy]-benzo[b]thiophen-7-yl}-propionic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

849150-59-0

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849150-59-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 849150-59-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,9,1,5 and 0 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 849150-59:
(8*8)+(7*4)+(6*9)+(5*1)+(4*5)+(3*0)+(2*5)+(1*9)=190
190 % 10 = 0
So 849150-59-0 is a valid CAS Registry Number.

849150-59-0Downstream Products

849150-59-0Relevant academic research and scientific papers

SOLID STATE FORMS OF ALEGLITAZAR SODIUM

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Paragraph 0067; 0068, (2014/01/07)

The present invention provides solid state forms of Aleglitazar sodium, processes for preparing the solid state forms, and pharmaceutical compositions comprising the solid state forms.

PROCESS FOR THE PREPARATION OF PROPIONIC ACID DERIVATIVES

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Page/Page column 23, (2011/06/26)

The invention relates to a process for the preparation of a compound of formula (I) or a salt thereof, by hydrogenation of a compound of formula (II).

PROCESS FOR THE PREPARATION OF PROPIONIC ACID DERIVATIVES

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Page/Page column 12, (2010/10/19)

The invention relates to a process for the preparation of a compound of formula (I) or a salt thereof.

Aleglitazar, a new, potent, and balanced dual PPARα/γ agonist for the treatment of type II diabetes

Benardeau, Agnes,Benz, Joerg,Binggeli, Alfred,Blum, Denise,Boehringer, Markus,Grether, Uwe,Hilpert, Hans,Kuhn, Bernd,Maerki, Hans Peter,Meyer, Markus,Puentener, Kurt,Raab, Susanne,Ruf, Armin,Schlatter, Daniel,Mohr, Peter

scheme or table, p. 2468 - 2473 (2010/03/24)

Design, synthesis, and SAR of novel α-alkoxy-β-arylpropionic acids as potent and balanced PPARαγ coagonists are described. One representative thereof, Aleglitazar ((S)-2Aa), was chosen for clinical development. Its X-ray structure in complex with both receptors as well as its high efficacy in animal models of T2D and dyslipidemia are also presented.

Process for the production of chiral propionic acid derivatives

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Page/Page column 10-11, (2010/02/11)

The present invention is concerned with a novel process for the preparation of compounds of formula I comprising catalytic asymmetric hydrogenation of a compound of formula (II) in the presence of a catalyst comprising ruthenium and a chiral diphosphine ligand or comprising rhodium and a chiral diphosphine ligand, wherein R1, R2, R3 and R4 are as defined in the specification and claims. The compounds of formula I and the corresponding salts and/or esters are pharmaceutically active substances.

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