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3-hydroxy-1-methyl-3-(naphthalen-2-yl)indolin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1309455-76-2

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1309455-76-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1309455-76-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,9,4,5 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1309455-76:
(9*1)+(8*3)+(7*0)+(6*9)+(5*4)+(4*5)+(3*5)+(2*7)+(1*6)=162
162 % 10 = 2
So 1309455-76-2 is a valid CAS Registry Number.

1309455-76-2Downstream Products

1309455-76-2Relevant academic research and scientific papers

Palladium-catalyzed asymmetric allylic alkylation of 3-aryloxindoles with allylidene dipivalate: A useful enol pivalate product

Trost, Barry M.,Masters, James T.,Burns, Aaron C.

, p. 2260 - 2264 (2013)

Triple A: The catalytic asymmetric allylic alkylation (AAA) of 3-aryloxindoles with allylidene dipivalate is described. This reaction affords stable, synthetically useful enol pivalates in high yield and with excellent regio- and enantioselectivity. A broad range of substrates is tolerated, including unprotected and 3-heteroaryl nucleophiles. Copyright

Photoredox asymmetric catalytic enantioconvergent substitution of 3-chlorooxindoles

Jiang, Zhiyong,Li, Yunqiang,Qiao, Baokun,Zeng, Guangkuo,Zhao, Xiaowei

supporting information, p. 11362 - 11365 (2019/09/30)

An enantioconvergent substitution of 3-substituted 3-chlorooxindoles with N-aryl glycines under visible light irradiation is reported. A transition-metal-free cooperative catalysis platform with a dicyanopyrazine-derived chromophore (DPZ) as a photoredox catalyst and a chiral Br?nsted acid catalyst is effective for these transformations, which involve a single-electron transfer redox step and an enantioselective radical coupling. A variety of valuable chiral 3-aminomethylene-3-substituted oxindoles can be directly synthesized with high yields and enantioselectivities.

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