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(E)-1-methyl-3-(3,3,3-trifluoro-1-nitroprop-1-en-2-yl)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1422985-00-9

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1422985-00-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1422985-00-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,2,9,8 and 5 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1422985-00:
(9*1)+(8*4)+(7*2)+(6*2)+(5*9)+(4*8)+(3*5)+(2*0)+(1*0)=159
159 % 10 = 9
So 1422985-00-9 is a valid CAS Registry Number.

1422985-00-9Relevant academic research and scientific papers

The squaramide-catalyzed asymmetric Michael/cyclization tandem reaction for the synthesis of chiral trifluoromethylated hydroxyimino tetrahydrobenzofuranones

Liu, Wei,Lai, Xiaoyan,Zha, Gaofeng,Xu, Yan,Sun, Panpan,Xia, Tao,Shen, Yongcun

supporting information, p. 3603 - 3607 (2016/04/19)

An enantioselective synthesis of trifluoromethylated hydroxyimino tetrahydrobenzofuranones has been developed. 1,3-Dicarbonyl carbocyclic compounds react with β-CF3-β-disubstituted nitroalkenes in the presence of a chiral squaramide catalyst, p

Enantioselective Michael Addition of Pyrazolin-5-ones to β-CF3-β-Disubstituted Nitroalkenes Catalyzed by Squaramide Organocatalyst

Lai, Xiaoyan,Zha, Gaofeng,Liu, Wei,Xu, Yan,Sun, Panpan,Xia, Tao,Shen, Yongcun

supporting information, p. 1983 - 1988 (2016/08/09)

A highly enantioselective Michael addition of pyrazolin-5-ones with β-CF3-β-disubstituted nitroalkenes catalyzed by bifunctional squaramide has been developed. Various chiral β-CF3-β-5-hydroxy-pyrazolin-3-yl-disubstituted nitroalkane derivatives bearing all-carbon quaternary stereocenter were prepared in good yields (up to 88%) and excellent enantioselectivities (up to 97% ee).

Enantioselective organocatalytic reduction of β-trifluoromethyl nitroalkenes: An efficient strategy for the synthesis of chiral β-trifluoromethyl amines

Massolo, Elisabetta,Benaglia, Maurizio,Orlandi, Manuel,Rossi, Sergio,Celentano, Giuseppe

supporting information, p. 3589 - 3595 (2015/03/04)

An efficient organocatalytic stereoselective reduction of β-trifluoromethyl-substituted nitroalkenes, mediated by 3,5-dicarboxylic ester-dihydropyridines (Hantzsch ester type), has been successfully developed. A multifunctional thiourea-based (S)-valine d

Highly enantioselective construction of trifluoromethylated all-carbon quaternary stereocenters via nickel-catalyzed friedel-crafts alkylation reaction

Gao, Jian-Rong,Wu, Hao,Xiang, Bin,Yu, Wu-Bin,Han, Liang,Jia, Yi-Xia

supporting information, p. 2983 - 2986 (2013/04/10)

A highly enantioselective Friedel-Crafts alkylation reaction of indoles with β-CF3-β-disubstituted nitroalkenes was achieved using a Ni(ClO4)2-bisoxazoline complex as a catalyst, which afforded indole-bearing chiral compou

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