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(2R,8R,9R)-(8-benzyloxy-9-benzyloxymethyl-4,8-dimethyl-2,3,6,7,8,9-hexahydro-oxonin-2-yl)-methanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

758716-31-3

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758716-31-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 758716-31-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,5,8,7,1 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 758716-31:
(8*7)+(7*5)+(6*8)+(5*7)+(4*1)+(3*6)+(2*3)+(1*1)=203
203 % 10 = 3
So 758716-31-3 is a valid CAS Registry Number.

758716-31-3Downstream Products

758716-31-3Relevant academic research and scientific papers

An intramolecular Diels-Alder approach to the eunicellins: Enantioselective total syntheses of ophirin B and astrogorgin

Crimmins, Michael T.,Brown, Brandon H.,Plake, Hilary R.

, p. 1371 - 1378 (2007/10/03)

The enantioselective syntheses of the eunicellins ophirin B and astrogorgin have been completed. Ring-closing metatheses provide efficient access to the oxonene rings, and highly diastereoselective intramolecular Diels-Alder reactions resulted in the form

A general strategy for synthesis of both (6Z)- and (6E)-cladiellin diterpenes: Total syntheses of (-)-cladiella-6,11-dien-3-ol, (+)-polyanthellin A, (-)-cladiell-11-ene-3,6,7-triol, and (-)-deacetoxyalcyonin acetate

Kim, Hyoungsu,Lee, Hyunjoo,Kim, Jayoung,Kim, Sanghee,Kim, Deukjoon

, p. 15851 - 15855 (2007/10/03)

The first total synthesis of an (E)-cladiellin diterpene, (-)-cladiella-6,11-diene-3-ol (1), was accomplished featuring an intramolecular amide enolate alkylation-intramolecular Diels-Alder strategy. In addition, a highly stereo-, regio-, and chemoselecti

Ah intramolecular Diels-Alder approach to the eunicelins: Enantioselective total synthesis of ophirin B

Crimmins, Michael T.,Brown, Brandon H.

, p. 10264 - 10266 (2007/10/03)

The enantioselective synthesis of the eunicellin ophirin B has been completed. A ring-closing metathesis provides efficient access to the oxonene ring, and a highly diastereoselective intramolecular Diels-Alder reaction results in the formation of the hyd

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