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(R)-(+)-6-(2-methoxynaphthalen-1-yl)-4,7-dimethyl-2-(toluene-4-sulfonyl)-2,3-dihydro-1H-isoindole-5-carboxylic acid isopropyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1198087-78-3

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1198087-78-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1198087-78-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,8,0,8 and 7 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1198087-78:
(9*1)+(8*1)+(7*9)+(6*8)+(5*0)+(4*8)+(3*7)+(2*7)+(1*8)=203
203 % 10 = 3
So 1198087-78-3 is a valid CAS Registry Number.

1198087-78-3Downstream Products

1198087-78-3Relevant academic research and scientific papers

Dendritic phosphoramidite ligands for Rh-catalyzed [2+2+2] cycloaddition reactions: Unprecedented enhancement of enantiodiscrimination

Garcia, Lidia,Roglans, Anna,Laurent, Regis,Majoral, Jean-Pierre,Pla-Quintana, Anna,Caminade, Anne-Marie

supporting information; experimental part, p. 9248 - 9250 (2012/09/11)

Phosphorus dendrimers containing terminal phosphoramidite ligands have been found to be highly effective and recoverable catalysts for the rhodium(i) catalyzed [2+2+2] cycloaddition reactions. A strong positive dendritic effect is observed both in the activity and enantiodiscrimination leading to axially chiral biaryl compounds.

Enantioselective synthesis of Axially chiral hydroxy carboxylic acid derivatives by rhodium-catalyzed [2 〈 2 〈 2] cycloaddition

Ogaki, Shuichiro,Shibata, Yu,Noguchi, Keiichi,Tanaka, Ken

supporting information; experimental part, p. 1926 - 1929 (2011/06/24)

Axially chiral hydroxy carboxylic acid derivatives were successfully synthesized with high yields and ee values by the cationic rhodium(I)/axially chiral biaryl bisphosphine complex-catalyzed enantioselective [2 〈 2 〈 2] cycloaddition. Axially chiral hydroxy and dihydroxy carboxylic acid derivatives, bearing the aryl group at the ortho-position of the alkoxycarbonyl group, were also synthesized with high regio- and enantioselectivity.

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