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(2S,3S,4R,5R,7R)-7-[(2S,3S,5S,7R,8S,9S)-7-(2-Benzyloxy-ethyl)-9-(tert-butyl-dimethyl-silanyloxy)-3-(4-methoxy-benzyloxy)-4,4,8-trimethyl-1,6-dioxa-spiro[4.5]dec-2-yl]-7-methoxy-2,4-dimethyl-heptane-1,3,5-triol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

218785-35-4

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218785-35-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 218785-35-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,8,7,8 and 5 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 218785-35:
(8*2)+(7*1)+(6*8)+(5*7)+(4*8)+(3*5)+(2*3)+(1*5)=164
164 % 10 = 4
So 218785-35-4 is a valid CAS Registry Number.

218785-35-4Upstream product

218785-35-4Relevant academic research and scientific papers

Total synthesis of (+)-calyculin A and (-)-calyculin B: Asymmetric synthesis of the C(9-25) spiroketal dipropionate subunit

Smith III, Amos B.,Friestad, Gregory K.,Barbosa, Joseph,Bertounesque, Emmanuel,Hull, Kenneth G.,Iwashima, Makoto,Qiu, Yuping,Salvatore, Brian A.,Spoors, P. Grant,Duan, James J.-W

, p. 10468 - 10477 (2007/10/03)

An asymmetric synthesis of the stereochemically fully endowed C(9-25) spiroketal fragment (+)-BC of the calyculins (1-8) is described. Highlights of the synthesis include: a highly diastereoselective IBr-induced iodocarbonate cyclization to introduce the

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