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4-methoxy-1,3-dihydro-2-benzofuran-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

130662-53-2

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130662-53-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 130662-53-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,6,6 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 130662-53:
(8*1)+(7*3)+(6*0)+(5*6)+(4*6)+(3*2)+(2*5)+(1*3)=102
102 % 10 = 2
So 130662-53-2 is a valid CAS Registry Number.

130662-53-2Relevant academic research and scientific papers

Squaramide-catalyzed asymmetric intramolecular oxa-michael reaction of α,β-unsaturated carbonyls containing benzyl alcohol: Construction of chiral 1-substituted phthalans

Son, Eun Chae,Kim, Seung Yeon,Kim, Sung-Gon

, p. 6826 - 6839 (2021/05/29)

Organocatalytic enantioselective intramolecular oxa-Michael reactions of benzyl alcohol bearing α,β-unsaturated carbonyls as Michael acceptors are presented herein. Using cinchona squaramide-based organocatalyst, enones as well as α,βunsaturated esters containing benzyl alcohol provided their corresponding 1,3-dihydroisobenzofuranyl-1-methylene ketones and 1,3-dihydroisobenzofuranyl-1-methylene esters in excellent yields with high enantioselectivities. In addition, enantioenriched 1,3-dihydroisobenzofuranyl-1-methylene ketone could be obtained from the Wittig/oxa-Michael reaction cascade of 1,3-dihydro-2-benzofuran-1-ol.

Organocatalytic enantioselective synthesis of phthalans via Wittig/oxa-Michael cascade reaction

Son, Eun Chae,No, Jaeeun,Kim, Sung-Gon

, p. 1473 - 1480 (2021/09/25)

An enantioselective synthetic method for 1-substituted phthalans has been developed. The organocatalytic reaction between 1,3-dihydro-2-benzofuran-1-ols and Wittig reagents using cinchona squaramide-based organocatalyst proceeded with sequential Wittig reaction followed by an enantioselective intramolecular oxa-Michael reaction, yielding enantioenriched phthalans with moderate to good enantioselectivities.

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