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methyl 2-(4-(1-oxoisoindolin-2-yl)phenyl)propanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

50712-44-2

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50712-44-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50712-44-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,7,1 and 2 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 50712-44:
(7*5)+(6*0)+(5*7)+(4*1)+(3*2)+(2*4)+(1*4)=92
92 % 10 = 2
So 50712-44-2 is a valid CAS Registry Number.

50712-44-2Downstream Products

50712-44-2Relevant academic research and scientific papers

GLC determination of indoprofen in plasma

Smith,Humphrey,Escalona Castillo

, p. 132 - 134 (1977)

Implementation of human bioavailability studies with the analgesic indoprofen required a rapid, sensitive, and convenient assay in blood plasma. A procedure based on ether extraction of acidified plasma, derivatization with diazomethane, and GLC analysis using a 3% OV 1 column was sufficiently sensitive for measurement of plasma indoprofen concentrations in the 0.4-16 μg/ml range. An average recovery of 99.0 ± 7.6% (SD) was achieved when the pentanoic acid homolog was employed as an internal standard.

Isoindolinone Synthesis: Selective Dioxane-Mediated Aerobic Oxidation of Isoindolines

Thapa, Pawan,Corral, Esai,Sardar, Sinjinee,Pierce, Brad S.,Foss, Frank W.

, p. 1025 - 1034 (2019/01/24)

N-Alkyl and N-aryl-isoindolinones were prepared by a dioxane-mediated oxidation of isoindoline precursors. The transformation exhibits unique chemoselectivity for isoindonlines. A chiral tertiary (3°)-benzylic position was not racemized during oxidation, and methyl indoprofen was prepared by late stage oxidation. Mechanistic studies suggest a selective H atom transfer, which avoids many known oxidation (by-)products of isoindolinones.

Transition metal free intramolecular selective oxidative C(sp3)-N coupling: Synthesis of N-aryl-isoindolinones from 2-alkylbenzamides

Verma, Ajay,Patel, Saket,Meenakshi,Kumar, Amit,Yadav, Abhimanyu,Kumar, Shailesh,Jana, Sadhan,Sharma, Shubham,Prasad, Ch. Durga,Kumar, Sangit

supporting information, p. 1371 - 1374 (2015/02/18)

A synthetic method has been developed for the preparation of biologically important isoindolinones including indoprofen and DWP205190 drugs from 2-alkylbenzamide substrates by transition metal-free intramolecular selective oxidative coupling of C(sp3)-H and N-H bonds utilizing iodine, potassium carbonate and di-tert-butyl peroxide in acetonitrile at 110-140 °C.

Lactam coupling as a versatile route to indoprofen analogs

Barnes, Keith D.,Chen, Ping,Chang, Yingyan,Lewis, Robert M.,Manley, Christopher M.,Mayhew, Nicholas J.,Steffke, Stephen H.,Wang, Guixing,Wang, Yi,Yang, Yuh-Lin A.,Lippert, John W.

experimental part, p. 67 - 72 (2011/03/19)

A convergent synthesis of indoprofen via a Buchwald coupling approach is reported. Using this methodology, indoprofen and a set of analogs of indoprofen were readily prepared. Copyright

METHODS AND COMPOSITIONS TO TREAT MOTOR NEURON DISEASE

-

Page/Page column 30, (2008/06/13)

The invention features compositions and methods for treating motor neuron diseases, such as spinal muscular atrophy and amyotrophic lateral sclerosis. The compositions and methods include derivatives of indoprofen.

Novel α-thio-alkanoic acid derivatives

-

, (2008/06/13)

Novel α-thio-alkanoic acid derivatives and a process for their preparation. These novel compounds can be easily converted to useful medicines.

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