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2H-Indol-2-one, 1,3-dihydro-3-[(4-methylphenyl)amino]-3-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

908150-31-2

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908150-31-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 908150-31-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,8,1,5 and 0 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 908150-31:
(8*9)+(7*0)+(6*8)+(5*1)+(4*5)+(3*0)+(2*3)+(1*1)=152
152 % 10 = 2
So 908150-31-2 is a valid CAS Registry Number.

908150-31-2Downstream Products

908150-31-2Relevant academic research and scientific papers

Synthesis of enantiomerically enriched 3-amino-2-oxindoles through a palladium-mediated asymmetric intramolecular arylation of α-ketimino amides

Tolstoy, Paeivi,Lee, Samantha X. Y.,Sparr, Christof,Ley, Steven V.

, p. 4810 - 4813,4 (2012/12/12)

A highly efficient and enantioselective synthesis of 3-amino-2-oxindoles through a palladium-catalyzed asymmetric intramolecular arylation of R-ketimino amides using (R)-DiFluorPhos as the coordinating ligand is reported. This report constitutes the first

Synthesis of enantiomerically enriched 3-amino-2-oxindoles through a palladium-mediated asymmetric intramolecular arylation of α-ketimino amides

Tolstoy, P?ivi,Lee, Samantha X.Y.,Sparr, Christof,Ley, Steven V.

, p. 4810 - 4813 (2013/01/15)

A highly efficient and enantioselective synthesis of 3-amino-2-oxindoles through a palladium-catalyzed asymmetric intramolecular arylation of R-ketimino amides using (R)-DiFluorPhos as the coordinating ligand is reported. This report constitutes the first

Thermal and acid-catalyzed Hofmann-Martius rearrangement of 3-N-aryl-2-oxindoles into 3-(arylamino)-2-oxindoles

Magnus, Philip,Turnbull, Rachel

, p. 3497 - 3499 (2007/10/03)

The Hofmann-Martius rearrangement of 3-N-aryl-2-oxindoles into 3-(arylamino)-2-oxindoles under thermal and acid-catalyzed conditions is described.

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