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(4aS,5R,6R,8aS)-5-(2,5-Dimethoxy-benzyl)-5,6,8a-trimethyl-octahydro-naphthalen-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

237735-95-4

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237735-95-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 237735-95-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,7,7,3 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 237735-95:
(8*2)+(7*3)+(6*7)+(5*7)+(4*3)+(3*5)+(2*9)+(1*5)=164
164 % 10 = 4
So 237735-95-4 is a valid CAS Registry Number.

237735-95-4Relevant academic research and scientific papers

Synthetic study of akaterpin: Determination of the relative stereochemistry of the upper decalin moiety with disulfated hydroquinone

Kawai, Nobuyuki,Takao, Ken-ichi,Kobayashi, Susumu

, p. 4193 - 4196 (2007/10/03)

In order to establish the stereochemistry of akaterpin, a specific inhibitor of PI-PLC, synthesis of cis-decalin 2 and trans-decalin 3 was carried out. Comparison of NMR spectra of 2 and 3 with that of akaterpin indicated that the upper decalin has a cis-fused structure.

Enantiospecific total synthesis of (+)- and (-)-avarone and -avarol

Locke, Edward P.,Hecht, Sidney M.

, p. 2717 - 2718 (2007/10/03)

Enantiopure avarol and its oxidized congener avarone are synthesized in both podal series from an optically pure Wieland-Miescher enone; preliminary results from biochemical studies are summarized.

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