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(+)-(αS,βR)-4,4'-dimethoxy-2'-O-methoxymethylchalcone epoxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

130322-31-5

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130322-31-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 130322-31-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,3,2 and 2 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 130322-31:
(8*1)+(7*3)+(6*0)+(5*3)+(4*2)+(3*2)+(2*3)+(1*1)=65
65 % 10 = 5
So 130322-31-5 is a valid CAS Registry Number.

130322-31-5Relevant academic research and scientific papers

Stereoselective synthesis of flavonoids. Part 7. Poly-oxygenated β- hydroxydihydrochalcone derivatives

Nel, Reinier J. J.,Van Rensburg, Hendrik,Van Heerden, Pieter S.,Coetzee, Johan,Ferreira, Daneel

, p. 9727 - 9736 (2007/10/03)

Epoxidation of a series of poly-oxygenated chalcones with urea-hydrogen peroxide complex in THF in the presence of DBU and poly-(L)- or -(D)-leucine, followed by TBTH/AIBN catalysed ring opening, afforded [β- hydroxydihydrochalcones in moderate to high en

Stereoselective synthesis of flavonoids. Part 4. Trans- and cis-dihydroflavonols

Van Rensburg, Hendrik,Van Heerden, Pieter S.,Bezuidenhoudt, Barend C.B.,Ferreira, Daneel

, p. 14141 - 14152 (2007/10/03)

Epoxidation of a series of poly-oxygenated chalcones with H2O2 in the presence of poly-α-aminoacids yielded chiral aromatic oxygenated oxiranes in moderate to high optical yields. Lewis acid-catalysed phenylmethanethiol ringopening o

The first enantioselective synthesis of trans- and cis-dihydroflavonols

Van Rensburg, Hendrik,Van Heerden, Pieter S.,Bezuidenhoudt, Barend C. B.,Ferreira, Daneel

, p. 2747 - 2748 (2007/10/03)

Epoxidation of a series of polyoxygenated chalcones with H2O2 in the presence of poly(α-amino acid) catalysts, followed by Lewis acid-catalysed phenylmethanethiol ring-opening and cyclization, afforded trans- and cis-dihydroflavonols

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