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4-(1H-indol-3-yl)-2-oxo-4-phenylbutyric acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1201664-92-7

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1201664-92-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1201664-92-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,1,6,6 and 4 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1201664-92:
(9*1)+(8*2)+(7*0)+(6*1)+(5*6)+(4*6)+(3*4)+(2*9)+(1*2)=117
117 % 10 = 7
So 1201664-92-7 is a valid CAS Registry Number.

1201664-92-7Downstream Products

1201664-92-7Relevant academic research and scientific papers

Enantioselective Friedel-Crafts alkylation of indoles with β,γ-unsaturated α-ketoesters catalyzed by new squaramide-linked bisoxazoline-Zn(OTf)2 complexes

Jia, Sheng-Jian,Du, Da-Ming

, p. 980 - 988 (2014/08/18)

Enantioselective Friedel-Crafts alkylation reactions of indoles with β,γ-unsaturated α-ketoesters catalyzed by novel chiral C 2-symmetric squaramide-linked bisoxazoline-Zn(OTf)2 complexes were investigated. The corresponding indole k

Optically active 1,1′-Spirobiindane-7,7′-diol (SPINOL)-based phosphoric acids as highly enantioselective catalysts for asymmetric organocatalysis

Xing, Chun-Hui,Liao, Yuan-Xi,Ng, Jaclynn,Hu, Qiao-Sheng

experimental part, p. 4125 - 4131 (2011/07/07)

The synthesis and application of a series of optically active 1,1′-spirobiindane-7,7′-diol (SPINOL)-based phosphoric acids are described. These SPINOL-based phosphoric acids were prepared from (R)-SPINOL in three steps and exhibited excellent enantioselec

Phosphonium ion tagged chiral phosphoric acids and their application in Friedel-Crafts reactions of indoles

Hermeke, Julia,Toy, Patrick H.

experimental part, p. 4103 - 4109 (2011/06/24)

The attachment of phosphonium ion phase tags to chiral binapthyl-based phosphoric acid catalysts, and the use of these materials in a range of organocatalytic asymmetric Friedel-Crafts reactions of indoles has been studied. Placement of the tags at the 3

AgAsF6/Sm(OTf)3 promoted reversal of enantioselectivity for the asymmetric Friedel-Crafts alkylations of indoles with β,γ-unsaturated α-ketoesters

Liu, Yanling,Shang, Deju,Zhou, Xin,Zhu, Yin,Lin, Liii,Liu, Xiaohua,Feng, Xiaoming

supporting information; experimental part, p. 180 - 183 (2010/05/18)

"Chemical Equation Presented" The first example of central metal controlled reversal of enantioselectivity in asymmetric Friedel-Crafts alkylation of indoles andβγ-unsaturated α-ketoesters has been developed. Using the same chiral starting material derive

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