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2-(3-methoxy-4-hydroxyphenyl)-7-methoxy-5-vinyl-2,3-dihydrobenzofuran is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

129504-74-1

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129504-74-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 129504-74-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,5,0 and 4 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 129504-74:
(8*1)+(7*2)+(6*9)+(5*5)+(4*0)+(3*4)+(2*7)+(1*4)=131
131 % 10 = 1
So 129504-74-1 is a valid CAS Registry Number.

129504-74-1Downstream Products

129504-74-1Relevant academic research and scientific papers

Cerium ammonium nitrate-mediated the oxidative dimerization of p-alkenylphenols: A new synthesis of substituted (±)-trans- dihydrobenzofurans

Chen, Po-Yuan,Wu, Yi-Hua,Hsu, Mon-Huei,Wang, Tzu-Pin,Wang, Eng-Chi

, p. 653 - 657 (2013/07/27)

A new method for the preparation of substituted dihydrobenzofurans is described. The p-alkenylphenols, mediated by cerium ammonium nitrate (CAN), undergo the oxidative dimerization to generate substituted dihydrobenzofurans including (±)-conocarpan, (±)-licarin A, (±)-acuminatin, as well as their related substituted dihydrobenzofurans.

Synthesis of enantiomerically enriched dimers of vinylphenols by tandem action of laccases and lipases

Gavezzotti, Paolo,Navarra, Cristina,Caufin, Stefania,Danieli, Bruno,Magrone, Pietro,Monti, Daniela,Riva, Sergio

experimental part, p. 2421 - 2430 (2011/11/04)

The tandem use of laccases and lipases has been exploited for the simple preparative synthesis of enantiomerically enriched dimeric phenols. Laccase-catalyzed oxidation of isoeugenol (1) and vinylguaiacol (7) in biphasic systems gave as main products the racemic compounds 6 and 8, possessing structures similar to the β-5 dimers found in lignin. The synthesis of enantiomerically enriched 6 and 8 could be achieved by alcoholysis reactions catalyzed by commercial preparations of lipases in organic solvents. Although the E values were quite low (due to the "remote" stereocenters to be discriminated), the enantio-complementary behavior of the tested lipases allowed the simple isolation of the target compounds with ee up to 90%. It is noteworthy that these results have been achieved in vitro exploiting commercially available enzymes, without using the so-called "dirigent" proteins evolved by nature to direct the enantioselective coupling of phenols in vivo. Copyright

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