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2,6-Bis(4-methoxyphenyl)-3,7-dioxabicyclo<3.3.0>octane-4,8-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69813-32-7

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69813-32-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69813-32-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,8,1 and 3 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 69813-32:
(7*6)+(6*9)+(5*8)+(4*1)+(3*3)+(2*3)+(1*2)=157
157 % 10 = 7
So 69813-32-7 is a valid CAS Registry Number.

69813-32-7Downstream Products

69813-32-7Relevant academic research and scientific papers

Reductive Bis-addition of Aromatic Aldehydes to α,β-Unsaturated Esters via the Use of Sm/Cu(I) in Air: A Route to the Construction of Furofuran Lignans

Liu, Yongjun,Tian, Guang,Li, Jingjing,Qi, Yan,Wen, Yonghong,Du, Feng

, p. 5932 - 5939 (2017/06/07)

The novel bis-addition of benzaldehydes to acrylates or maleates was achieved by the direct use of samarium metal with the assistance of CuI under mild conditions under dry air, and the useful 2-hydroxylalkyl-γ-butyrolactons and lignan derivatives were thus constructed with high efficiency. The key factors that influence the reaction efficiency were investigated. The use of potassium iodide and molecular sieves as additives can improve the reaction efficiency remarkably.

Electochemical asymmetric dimerization of cinnamic acid derivatives and application to the enantioselective syntheses of furofuran lignans

Mori, Naoki,Furuta, Akiko,Watanabe, Hidenori

, p. 8393 - 8399 (2016/12/06)

A new electrochemical method for the asymmetric oxidative dimerization of cinnamic acid derivatives has been developed. This method enabled the enantioselective syntheses of furofuran lignans, yangambin, sesamin and eudesmin.

Reactions of Trialkylsilyl Trifluoromethanesulfonates, XII. - Aldol-Type Reactions with 2,6-Bis(trimethylsilyloxy)thiophene Synthesis of Bicyclic γ-Lactones

Rzehak, Werner,Simchen, Gerhard

, p. 615 - 620 (2007/10/02)

In the presence of trimethylsilyl triflate (2) aromatic aldehydes 4 react with 2,6-bis(trimethylsilyloxy)thiophene (3) to yield the 3,4-disubstituted thiosuccinic anhydrides 5.By hydrolysis of the products 5 in the presence of lead acetate the diaryl-subs

Thallium in Organic Synthesis. 60. 2,6-Diaryl-3,7-dioxabicyclooctane-4,8-dione Lignans by Oxidative Dimerization of 4-Alkoxycinnamic Acids with Thallium(III) Trifluoroacetate or Cobalt(III) Trifluoride

Taylor, Edward C.,Andrade, Juan G.,Rall, Gerhardus J.H.,Steliou, Kosta,Jagdmann, G. Erik,McKillop, Alexander

, p. 3078 - 3081 (2007/10/02)

Oxidation of p-alkoxycinnamic acids either with thallium(III) trifluoroacetate in TFA/CH2Cl2 or with cobalt(III) trifluoride in CH3CN, in the presence of a small amount of BF3*Et2O, results in instantaneous oxidative dimerization to give the bislactone li

CHEMISTRY OF 2,5-BIS(TRIMETHYLSILOXY)FURANS. II: REACTIONS WITH CARBONYL COMPOUNDS AND THE SYNTHESIS OF 2,6-DIARYL-3,7-DIOXABICYCLOOCTANE-4,8-DIONES

Brownbridge, Peter,Chan, Tak-Hang

, p. 3427 - 3430 (2007/10/02)

2,5-Bis(trimethylsiloxy)furan reacted with a number of substituted benzaldehydes under activation of titan tetrachloride to give 2,6-diaryl-3,7-dioxabicyclooctane-4,8-diones.

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