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(E)-3-(2-(1,3-dioxolan-2-yl)phenyl)-1-(4-methoxyphenyl)prop-2-en-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1431986-50-3

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1431986-50-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1431986-50-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,3,1,9,8 and 6 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1431986-50:
(9*1)+(8*4)+(7*3)+(6*1)+(5*9)+(4*8)+(3*6)+(2*5)+(1*0)=173
173 % 10 = 3
So 1431986-50-3 is a valid CAS Registry Number.

1431986-50-3Relevant academic research and scientific papers

Cobalt-Catalyzed Chemoselective Transfer Hydrogenative Cyclization Cascade of Enone-Tethered Aldehydes

Ma, Shuang-Shuang,Jiang, Biao-Ling,Yu, Zheng-Kun,Zhang, Suo-Jiang,Xu, Bao-Hua

, p. 3873 - 3878 (2021/05/26)

The ligand-free Co-catalyzed chemoselective reductive cyclization cascade of enone-tethered aldehydes with i-PrOH as the environmentally benign hydrogen surrogate is developed by this study. Mechanistic studies disclosed that such a protocol is initiated

Organocatalytic, Enantioselective, intramolecular oxa-michael reaction of alkoxyboronate: A new strategy for enantioenriched 1-substituted 1,3-Dihydroisobenzofurans

Ravindra, Barnala,Das, Braja Gopal,Ghorai, Prasanta

, p. 5580 - 5583 (2015/02/19)

An unprecedented strategy for the synthesis of enantioenriched 1-substituted 1,3-dihydroisobenzofurans via an enantioselective oxa-Michael reaction of o-alkoxyboronate containing chalcone (II) has been accomplished employing cinchona alkaloid based squara

Stereoselective synthesis of aminoindanols via an efficient cascade aza-Michael-aldol reaction

Qian, Hui,Zhao, Wanxiang,Sung, Herman H-Y.,Williams, Ian D.,Sun, Jianwei

supporting information, p. 4361 - 4363 (2013/06/05)

An efficient organocatalyzed strategy for the synthesis of 3-amino-1-indanols has been developed. This method is complementary to the conventional Friedel-Crafts strategy. It is also applicable to the synthesis of enantioenriched 3-amino-1-indanols.

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