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Butanoic acid, 2-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-4-[(1-phenyl-1H-tetrazol-5-yl)sulf onyl]-, 5-methyl-2-methylenehexyl ester, (2S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

398517-13-0

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398517-13-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 398517-13-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,9,8,5,1 and 7 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 398517-13:
(8*3)+(7*9)+(6*8)+(5*5)+(4*1)+(3*7)+(2*1)+(1*3)=190
190 % 10 = 0
So 398517-13-0 is a valid CAS Registry Number.

398517-13-0Downstream Products

398517-13-0Relevant academic research and scientific papers

Lasonolide A: Structural revision and total synthesis

Song, Ho Young,Joo, Jung Min,Kang, Jung Won,Kim, Dae-Shik,Jung, Cheol-Kyu,Kwak, Hyo Shin,Park, Jin Hyun,Lee, Eun,Hong, Chang Yong,Jeong, ShinWu,Jeon, Kiwan

, p. 8080 - 8087 (2007/10/03)

The proposed structure of lasonolide A was synthesized employing radical cyclization reactions of β-alkoxyacrylates for preparation of the tetrahydropyranyl units A and B, but the spectroscopic data did not match those of the natural product. Both enantio

Lasonolide A: Structural revision and synthesis of the unnatural (-)-enantiomer

Lee, Eun,Ho, Young Song,Jung, Won Kang,Kim, Dae-Shik,Jung, Cheol-Kyu,Jung, Min Joo

, p. 384 - 385 (2007/10/03)

Total synthesis of the unnatural (-)-enantiomer of lasonolide A was achieved starting from ethyl l-malate. The two tetrahydropyranyl fragments were prepared stereoselectively via radical cyclization reactions of β-alkoxyacrylates. The full structure of na

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