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2-(2-oxo-3-(2-oxo-2-phenylethyl)indolin-3-yl)malononitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75459-97-1

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75459-97-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75459-97-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,4,5 and 9 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 75459-97:
(7*7)+(6*5)+(5*4)+(4*5)+(3*9)+(2*9)+(1*7)=171
171 % 10 = 1
So 75459-97-1 is a valid CAS Registry Number.

75459-97-1Downstream Products

75459-97-1Relevant academic research and scientific papers

Molecular sieve mediated sequential Knoevenagel condensation/decarboxylative Michael addition reaction: Efficient and mild conditions for the synthesis of 3,3-disubstituted oxindoles with an all carbon quaternary center

Guo, Yi-Lin,Li, Yu-Hsun,Chang, Hsuan-Hao,Kuo, Ting-Shen,Han, Jeng-Liang

, p. 74683 - 74690 (2016)

A one-pot, molecular sieve mediated sequential Knoevenagel condensation/decarboxylative Michael addition reaction has been developed. We discovered that the molecular sieves not only promoted the Knoevenagel condensation of isatins and malononitrile to generate isatylidene malononitriles, but also promoted the later decarboxylative Michael addition reactions of β-ketoacids and malonic acid half thioesters (MAHTs) with isatylidene malononitriles. This protocol provides a mild and efficient method for the preparation of 3,3-disubstituted oxindoles with an all carbon quaternary center in high yields.

Grinding assisted, column chromatography free decarboxylative carbon-carbon bond formation: Greener synthesis of 3, 3-disubstituted oxindoles

Kaur, Jasneet,Kumari, Anita,Chimni, Swapandeep Singh

, p. 802 - 808 (2017)

The decarboxylative carbon-carbon bond formation reaction of β-ketoacid derivatives with isatylidene malononitrile derivatives catalyzed by DBU afford adducts in excellent yield. The desired product can be easily isolated using simple filtration method without performing any column chromatography. The decarboxylative adduct was further subjected to reductive-cyclization to obtain biologically important spirooxindoles in 89% yield.

Spiro Heterocyclic Compounds. IV. Synthesis of Spiro and Spiro Compounds

Higashiyama, Kimio,Otamasu, Hirotaka

, p. 1540 - 1545 (2007/10/02)

The Michael reaction of 3-(carboethoxy-cyano)methyleneoxindole (Ia) or 3-dicyanomethyleneoxindole (Ib) with active methyl groups, e.g., acetophenone and acetone, afforded, the corresponding normal Michael adducts (IIa-c).The reduction of IIa with NaBH4 ga

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