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60859-72-5

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60859-72-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60859-72-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,8,5 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 60859-72:
(7*6)+(6*0)+(5*8)+(4*5)+(3*9)+(2*7)+(1*2)=145
145 % 10 = 5
So 60859-72-5 is a valid CAS Registry Number.

60859-72-5Relevant academic research and scientific papers

Catalytic Enantioselective Synthesis of 3,4,5-Trisubstituted Isoxazoline N-Oxides and Regioselective Synthesis of 3,4,5-Trisubstituted Isoxazoles

Sahoo, Subas Chandra,Pan, Subhas Chandra

supporting information, p. 1385 - 1389 (2019/01/09)

An efficient catalytic asymmetric synthesis of 3,4,5-trisubstituted isoxazoline N-oxides and regioselective synthesis of 3,4,5-trisubstituted isoxazoles has been described. α-Nitrocinnamates and α-nitrobenzophenones were utilized as Michael acceptors resp

Direct aziridination of nitroalkenes affording N-alkyl-C-nitroaziridines and the subsequent Lewis acid mediated isomerization to β-nitroenamines

Hao, Feiyue,Asahara, Haruyasu,Nishiwaki, Nagatoshi

supporting information, p. 5442 - 5445 (2017/11/06)

A mild and highly diastereoselective one-pot synthesis of trans-N-alkyl-C-nitroaziridines was achieved by treatment of nitroalkenes with aliphatic amines and N-chlorosuccinimide. Treatment of the obtained aziridines with a Lewis acid resulted in a facile ring opening reaction, accompanied by rearrangement and isomerization into functionalized (Z)-β-nitroenamines.

Nucleophilic addition to nitroacrylates: application towards the synthesis of 2,3-dehydroamino acids and 2,3-diamino acids

Lewandowska, Elzbieta,Wichlacz, Kinga,Sobczak, Adam J.

body text, p. 152 - 156 (2010/03/01)

The addition of the N-pronucleophiles to 2- or 3-nitro-2-alkenoates in the presence of base provided Michael addition products. In the case of 3-nitro compounds, reaction occurred via the formation of α-adducts and the subsequent elimination of nitrous ac

Catalytic and asymmetric Friedel-Crafts alkylation of indoles with nitroacrylates. Application to the synthesis of tryptophan analogues

Sui, Yong,Liu, Li,Zhao, Jun-Ling,Wang, Dong,Chen, Yong-Jun

, p. 5173 - 5183 (2008/02/01)

An asymmetric Friedel-Crafts alkylation of indoles with nitroacrylates catalyzed by chiral (4R,5S)-DiPh-BOX (L1)-Cu(OTf)2 complex (10 mol %) has been developed. The reactions provide tryptophan nitro-precursors in moderate diastereoselectivitie

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