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Benzeneacetic acid, (3S,6E)-3-hydroxy-3,7,11-trimethyl-6,10-dodecadienyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

851050-91-4

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851050-91-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 851050-91-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,1,0,5 and 0 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 851050-91:
(8*8)+(7*5)+(6*1)+(5*0)+(4*5)+(3*0)+(2*9)+(1*1)=144
144 % 10 = 4
So 851050-91-4 is a valid CAS Registry Number.

851050-91-4Relevant academic research and scientific papers

Biomimetic synthesis of acid-sensitive (-)-caparrapi oxide and (+)-8-epicaparrapi oxide induced by artificial cyclases

Uyanik, Muhammet,Ishibashi, Hideaki,Ishihara, Kazuaki,Yamamoto, Hisashi

, p. 1601 - 1604 (2007/10/03)

(Chemical Equation Presented) Asymmetric total syntheses of acid-sensitive (-)-caparrapi oxide (1) and (+)-8-epicaparrapi oxide (2) from farnesol (9) were achieved using Sharptess-Katsuki epoxidation and Lewis acid-assisted chiral Bronsted acid (chiral LBA)-induced polyene cyclization as key steps. Furthermore, (-)-1 could be directly synthesized from (S)-nerolidol (3) and (R)-LBA with 88% ds by reagent control which overcame substrate control, while (-)-2 was obtained from (R)-3 and (R)-LBA with >99% ds by the double-asymmetric induction.

Biomimetic synthesis of acid-sensitive (-)- and (+)-caparrapi oxides, (-)- and (+)-8-epicaparrapi oxides, and (+)-dysifragin induced by artificial cyclases

Uyanik, Muhammet,Ishihara, Kazuaki,Yamamoto, Hisashi

, p. 5055 - 5065 (2007/10/03)

Asymmetric total syntheses of acid-sensitive (-)- and (+)-caparrapi oxides (1) and (+)-8-epicaparrapi oxide (2) from farnesol (10) are achieved using Sharpless-Katsuki epoxidation and Lewis acid-assisted chiral Bronsted acid (chiral LBA)-induced polyene cyclization as key steps. The relative configuration of (+)-dysifragin (4) is determined by a single-crystal X-ray diffraction and its total synthesis is accomplished by the diastereoselective epoxidation of (+)-1. Furthermore, (-)-1 can be directly synthesized from (S)-nerolidol (3) and (R)-LBA with 88% ds by reagent control, which overcame substrate control, while (-)-2 is obtained from (R)-3 and (R)-LBA with >99% ds by the double asymmetric induction.

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