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(S)-4-Benzyloxy-1-{(2S,6R)-4-[2-(tert-butyl-dimethyl-silanyloxy)-eth-(Z)-ylidene]-6-vinyl-tetrahydro-pyran-2-yl}-5-{(4R,6S)-6-[2-(tert-butyl-diphenyl-silanyloxy)-ethyl]-2,2-dimethyl-[1,3]dioxan-4-yl}-3,3-dimethyl-pentan-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

884345-36-2

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884345-36-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 884345-36-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,4,3,4 and 5 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 884345-36:
(8*8)+(7*8)+(6*4)+(5*3)+(4*4)+(3*5)+(2*3)+(1*6)=202
202 % 10 = 2
So 884345-36-2 is a valid CAS Registry Number.

884345-36-2Relevant academic research and scientific papers

The evolution of a stereoselective synthesis of the C1-C16 fragment of bryostatins

Ball, Matthew,Baron, Anne,Bradshaw, Ben,Dumeunier, Rapha?l,O'Brien, Matthew,Thomas, Eric J.

, p. 9650 - 9681 (2016/10/22)

The development of a synthesis of the C1-C16 fragment of bryostatins in which the key step is a stereoselective oxy-Michael reaction used to assemble the cis-2,6-disubstituted tetrahydropyran with the exocyclic alkene already installed, is described. Foll

A preliminary evaluation of a metathesis approach to bryostatins

Ball, Matthew,Bradshaw, Benjamin J.,Dumeunier, Rapha?l,Gregson, Thomas J.,MacCormick, Somhairle,Omori, Hiroki,Thomas, Eric J.

, p. 2223 - 2227 (2007/10/03)

Preliminary investigations into the synthesis of bryostatins using ring-closing metathesis to form the C(16)-C(17) double bond led to a synthesis of the bryostatin analogue 51; precursors 26 and 52, which possess the geminal dimethyl group at C-18, did no

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