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methyl (1R)-1-[2-(3-isopropyl-1-methyl-2-{[(trifluoromethyl)sulfonyl]oxy}cyclopent-2-en-1-yl)ethyl]-4-oxocyclohexa-2,5-diene-1-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

868615-39-8

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868615-39-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 868615-39-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,8,6,1 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 868615-39:
(8*8)+(7*6)+(6*8)+(5*6)+(4*1)+(3*5)+(2*3)+(1*9)=218
218 % 10 = 8
So 868615-39-8 is a valid CAS Registry Number.

868615-39-8Downstream Products

868615-39-8Relevant academic research and scientific papers

Synthetic studies on cyathin terpenoids: Enantioselective synthesis of the tricyclic core of cyathin through intramolecular Heck cyclisation

Drege, Emmanuelle,Tominiaux, Cyrille,Morgant, Georges,Desmaele, Didier

, p. 4825 - 4840 (2007/10/03)

An enantioselective synthesis of the tricyclic ketone (+)-5, which displays the carbon core of NGF-inducing cyathane diterpenes, has been completed according to a strategy in which the key step was the intramolecular Heck reaction of the AC subunit 49 est

Asymmetric synthesis of the tricyclic core of cyathin diterpenoids via intramolecular Heck reaction

Drège, Emmanuelle,Morgant, Georges,Desma?le, Didier

, p. 7263 - 7266 (2007/10/03)

The enantioselective synthesis of the ketones 3 which displays the carbon core of NGF-inducing cyathane diterpenes is described. The key tricyclic trienone 22 was assembled in 13 steps from Michael adduct (R)-8a via intramolecular Heck cyclization of the

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